@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_head { this: np:hasAssertion dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_assertion; np:hasProvenance dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_provenance; np:hasPublicationInfo dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_publicationInfo; a np:Nanopublication . dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_assertion a np:Assertion . dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_provenance a np:Provenance . dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_publicationInfo a np:PublicationInfo . } dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_assertion { miriam-gene:5554 a ncit:C16612 . lld:C2584620 a ncit:C7057 . dgn-gda:DGN8968e4cc084dc6e3e1f6c9b915677c0e sio:SIO_000628 miriam-gene:5554, lld:C2584620; a sio:SIO_001121 . } dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_provenance { dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_assertion dcterms:description "[These observations extend recent evidence of an increased thrombotic risk conferred by the coexistence of heterozygous PC deficiency and heterozygous activated PC resistance and support the paradigm in which hereditary thrombophilia is often a multigenic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:8704244; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1353719.RAGnYHXGLRrGQHWP2YVZ4LAkpGiu-cXiHD3dAJNJIz05I130_publicationInfo { this: dcterms:created "2016-05-13T12:51:59+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }