@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:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_head { this: np:hasAssertion dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_assertion; np:hasProvenance dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_provenance; np:hasPublicationInfo dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_publicationInfo; a np:Nanopublication . dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_assertion a np:Assertion . dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_provenance a np:Provenance . dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_publicationInfo a np:PublicationInfo . } dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_assertion { miriam-gene:2153 a ncit:C16612 . lld:C0032914 a ncit:C7057 . dgn-gda:DGNbccd226e7dbc167d44a7955dfe80e6bc sio:SIO_000628 miriam-gene:2153, lld:C0032914; a sio:SIO_001122 . } dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_provenance { dgn-np:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_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:NP167043.RANs9PYS-vCr8uXTE8JgpO-_RmQLPgkdAJJhQL7DCZ8ds130_publicationInfo { this: dcterms:created "2016-05-13T12:43:03+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" . }