http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#head http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#assertion http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#provenance http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#assertion http://rdf.disgenet.org/resource/gda/DGN71c36e097dbe6ec508338d37224df853 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/1351 http://rdf.disgenet.org/resource/gda/DGN71c36e097dbe6ec508338d37224df853 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1282975 http://rdf.disgenet.org/resource/gda/DGN71c36e097dbe6ec508338d37224df853 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#provenance http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#assertion http://purl.org/dc/terms/description [The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#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/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/9684781 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#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/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/dc/terms/created 2017-10-17T13:11:42+02:00 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP235834.RAwv48kxrMTHWPTf9nHQCBiNellKNDxC_6XVsg5fUsPRE 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