@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:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_head { this: np:hasAssertion dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_assertion; np:hasProvenance dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_provenance; np:hasPublicationInfo dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_publicationInfo; a np:Nanopublication . dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_assertion a np:Assertion . dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_provenance a np:Provenance . dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_publicationInfo a np:PublicationInfo . } dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_assertion { miriam-gene:2153 a ncit:C16612 . lld:C0000786 a ncit:C7057 . dgn-gda:DGN346141170dfec99d7495c931fec51f52 sio:SIO_000628 miriam-gene:2153, lld:C0000786; a sio:SIO_001122 . } dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_provenance { dgn-np:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_assertion dcterms:description "[Known mutations and novel SNPs in the factor V gene were identified in the study cohort determined to have APCR in pregnancy. Further studies are required to investigate the contribution of these novel SNPs to the APCR phenotype. Adverse outcomes includin]. 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:20214832; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP140126.RAMKA6cRO_9j9OjS2vTvZAlo2yjqyODiJed4WkLIDrc4A130_publicationInfo { this: dcterms:created "2015-08-25T14:38:58+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }