@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:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_head { this: np:hasAssertion dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_assertion; np:hasProvenance dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_provenance; np:hasPublicationInfo dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_publicationInfo; a np:Nanopublication . dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_assertion a np:Assertion . dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_provenance a np:Provenance . dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_assertion { miriam-gene:5979 a ncit:C16612 . lld:C0025269 a ncit:C7057 . dgn-gda:DGNd80a05e7860d35afb1652b33f3f959eb sio:SIO_000628 miriam-gene:5979, lld:C0025269; a sio:SIO_001121 . } dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_provenance { dgn-np:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_assertion dcterms:description "[DNA sequence analysis showed that none of the affected individuals had mutations in either exon 10 or 11, or in exon 16 of the RET protooncogene, regions where mutations have been described for MEN type 2A (MEN-2A) and MEN-2B families, respectively.]. 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:7829628; 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:NP1323189.RAbkjFRuy5mK1IVtmW2-wCms6CYmVtdW0lSoUOMJgJHB8130_publicationInfo { this: dcterms:created "2016-05-13T12:51:46+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" . }