@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:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_head { this: np:hasAssertion dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_assertion; np:hasProvenance dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_provenance; np:hasPublicationInfo dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_publicationInfo; a np:Nanopublication . dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_assertion a np:Assertion . dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_provenance a np:Provenance . dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_assertion { miriam-gene:5009 a ncit:C16612 . lld:C0268542 a ncit:C7057 . dgn-gda:DGN3ba445192372155cc2ff832d1e2aace4 sio:SIO_000628 miriam-gene:5009, lld:C0268542; a sio:SIO_001121 . } dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_provenance { dgn-np:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_assertion dcterms:description "[By analysing the restriction fragment length polymorphism (RFLP) detected by an ornithinetranscarbamylase (OTC) gene specific DNA probe, we followed the segregation of the defective gene in two families with OTC deficiency (X-linked disease).]. 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:2899508; 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:NP1298157.RAw4SJrN6fUNbD1uKkNPcq7ldP2wIi4kNthNbXp3TRBZU130_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" . }