@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:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_head { this: np:hasAssertion dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_assertion; np:hasProvenance dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_provenance; np:hasPublicationInfo dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_publicationInfo; a np:Nanopublication . dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_assertion a np:Assertion . dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_provenance a np:Provenance . dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_assertion { miriam-gene:6768 a ncit:C16612 . lld:C0684275 a ncit:C7057 . dgn-gda:DGNe2f5c8fb8a9edb33f117b2f08ca6e196 sio:SIO_000628 miriam-gene:6768, lld:C0684275; a sio:SIO_001121 . } dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_provenance { dgn-np:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_assertion dcterms:description "[The haplotypes generated by two extra-genic RFLPs, at DXS52 (St14/Taq1) and DXS15 (DX13/BglII), and one intragenic RFLP in F8C (647/BclI) indicated that: she was not a carrier; the case of hemophilia resulted from a de novo mutation in a grandfather's gamete.]. 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:2877941; 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:NP1297742.RAj9T6uO7Lu-l9bkMwr1vcZ-wix2Auk3IIYKOFtKKl2XY130_publicationInfo { this: dcterms:created "2016-05-13T12:51:34+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" . }