@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:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_head { this: np:hasAssertion dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_assertion; np:hasProvenance dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_provenance; np:hasPublicationInfo dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_publicationInfo; a np:Nanopublication . dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_assertion a np:Assertion . dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_provenance a np:Provenance . dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_publicationInfo a np:PublicationInfo . } dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_assertion { miriam-gene:5555 a ncit:C16612 . lld:C0398623 a ncit:C7057 . dgn-gda:DGN376cbf80ce47c6239c486cca18304564 sio:SIO_000628 miriam-gene:5555, lld:C0398623; a sio:SIO_001121 . } dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_provenance { dgn-np:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_assertion dcterms:description "[Detailed investigations of thrombophilia showed that four patients were positive for antiphospholipid antibodies, one of whom was also homozygous for the plasminogen-activator inhibitor-1 4G/4G polymorphism, and the fifth patient was deficient for protein C. Despite the concomitant presence of both coagulation factor defect and thrombophilia, fetal loss may be attributed to factor defect that in reality is a red herring, with underlying thrombophilia not being evaluated.]. 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:17762534; 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:NP627610.RA_BkT8nTXDCkJ3f6t2_Gbkrj0YsVkNRXJIm1ZzpwA2fA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:30+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" . }