http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#head http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#assertion http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#provenance http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#assertion http://rdf.disgenet.org/resource/gda/DGN23a511defd7c1b49cad41c6d338c65de http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/100048912 http://rdf.disgenet.org/resource/gda/DGN23a511defd7c1b49cad41c6d338c65de http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1956346 http://rdf.disgenet.org/resource/gda/DGN23a511defd7c1b49cad41c6d338c65de http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#provenance http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#assertion http://purl.org/dc/terms/description [Our thorough genomic characterization of 9p21.3 suggests common variants likely account for observed disease associations and provides further support for the hypothesis that complex regulatory variation affecting ANRIL and CDKN2B gene expression may contribute to increased risk for clinically apparent and subclinical coronary artery disease and aortic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#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/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/23315372 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#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/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/dc/terms/created 2017-10-17T13:19:27+02:00 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1459196.RAuonzfZY7hAC_uDoCg-LhrNea6kttjWMUGqrUUAuXlCo 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