http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#head http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#assertion http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#provenance http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#assertion http://rdf.disgenet.org/resource/gda/DGNf00a7aab979c877638feafbc5f1ed9c8 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4137 http://rdf.disgenet.org/resource/gda/DGNf00a7aab979c877638feafbc5f1ed9c8 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C3887938 http://rdf.disgenet.org/resource/gda/DGNf00a7aab979c877638feafbc5f1ed9c8 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#provenance http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#assertion http://purl.org/dc/terms/description [Recent studies have detected an over-representation of the H1 haplotype of the MAPT gene in neurodegenerative disorders such as progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), frontotemporal dementia (FTD) and Parkinson's disease (PD), whereas the H2 haplotype has been found to be related to familial FTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#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/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18854867 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#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/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/dc/terms/created 2017-10-17T13:14:25+02:00 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP664347.RAY9tuY1huUq-cHOGhIdSULkG1FkI9IAhchwtdJHydyH4 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