@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:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_head { this: np:hasAssertion dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_assertion; np:hasProvenance dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_provenance; np:hasPublicationInfo dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_publicationInfo; a np:Nanopublication . dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_assertion a np:Assertion . dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_provenance a np:Provenance . dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_publicationInfo a np:PublicationInfo . } dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_assertion { miriam-gene:2147 a ncit:C16612 . lld:C0004153 a ncit:C7057 . dgn-gda:DGNd8bff5a3370645fe12e74565a0f83e95 sio:SIO_000628 miriam-gene:2147, lld:C0004153; a sio:SIO_001122 . } dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_provenance { dgn-np:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_assertion dcterms:description "[In conclusion, our data suggest that FII G20210A and/or Leiden FV might be involved as risk factor for arterial disorders in about 5% of old subjects, justifying the opportunity of a genetic screening and an eventual preventive treatment, in particular in old subjects in which other and major risk factors, as hypertension and atherosclerosis, are detected.]. 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:21918818; 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:NP923963.RAPPNqn-i5Rja-Ai7umNr2pCckpJzMECT8wVLXmffiQYY130_publicationInfo { this: dcterms:created "2016-05-13T12:48:43+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" . }