http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#head http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#provenance http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://rdf.disgenet.org/resource/gda/DGN40a0a16d8cc19cbec93200a0c6861076 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4137 http://rdf.disgenet.org/resource/gda/DGN40a0a16d8cc19cbec93200a0c6861076 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0338451 http://rdf.disgenet.org/resource/gda/DGN40a0a16d8cc19cbec93200a0c6861076 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#provenance http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://purl.org/dc/terms/description [The aim of the present study is to investigate UPR activation in sporadic tauopathies like progressive supranuclear palsy (PSP) and Pick's disease (PiD), and familial cases with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) which carry mutations in the gene encoding for tau (MAPT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/22102449 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/dc/terms/created 2017-10-17T13:14:25+02:00 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP665190.RA2zX6e2sJrdLe7S3b7fQe0lT_GPvOLmMEb2Rki8BQToA http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0