@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:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_head { this: np:hasAssertion dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion; np:hasProvenance dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance; np:hasPublicationInfo dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_publicationInfo; a np:Nanopublication . dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion a np:Assertion . dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance a np:Provenance . dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_publicationInfo a np:PublicationInfo . } dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion { miriam-gene:1027 a ncit:C16612 . lld:C0032000 a ncit:C7057 . dgn-gda:DGN9494006c36fa444c3bc318f8bc2e0f7d sio:SIO_000628 miriam-gene:1027, lld:C0032000; a sio:SIO_001121 . } dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_provenance { dgn-np:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_assertion dcterms:description "[Such rare CDKN1B variants may contribute to the development of pituitary adenomas, but their low incidence and lack of clear segregation with affected patients make CDKN1B sequencing unlikely to be of use in routine genetic investigation of FIPA kindreds.]. 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:22291433; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP303392.RAvDa15CK8qljcI9cMnass-Mj-YShMhKR204D3XJjcwyU130_publicationInfo { this: dcterms:created "2015-08-25T14:40:34+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }