@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:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_head { this: np:hasAssertion dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_assertion; np:hasProvenance dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_provenance; np:hasPublicationInfo dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_publicationInfo; a np:Nanopublication . dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_assertion a np:Assertion . dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_provenance a np:Provenance . dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_publicationInfo a np:PublicationInfo . } dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_assertion { miriam-gene:2243 a ncit:C16612 . lld:C0001733 a ncit:C7057 . dgn-gda:DGN81da772ca562ad0377f2d57a0c6c9087 sio:SIO_000628 miriam-gene:2243, lld:C0001733; a sio:SIO_001122 . } dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_provenance { dgn-np:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_assertion dcterms:description "[Here we report the identification and functional analysis of a novel nonsense mutation in FGA exon 5: c.718C>T (CAG>TAG) p.Q240X (Q221X in the mature chain lacking the signal peptide), accounting for fibrinogen deficiency in six Egyptian patients.]. 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:20051841; 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:NP785131.RAmm04SsJfbRxH_aEJILnKApiS8v_uuqwOeuzOHMdLHcA130_publicationInfo { this: dcterms:created "2016-05-13T12:47:41+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" . }