@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:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_head { this: np:hasAssertion dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_assertion; np:hasProvenance dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_provenance; np:hasPublicationInfo dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_publicationInfo; a np:Nanopublication . dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_assertion a np:Assertion . dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_provenance a np:Provenance . dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_publicationInfo a np:PublicationInfo . } dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_assertion { miriam-gene:805 a ncit:C16612 . lld:C1833372 a ncit:C7057 . dgn-gda:DGNb51e0a55dd32993610ecd4c2d8081a4f sio:SIO_000628 miriam-gene:805, lld:C1833372; a sio:SIO_001121 . } dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_provenance { dgn-np:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_assertion dcterms:description "[The calmodulin III gene is located within this interval, and DNA sequence analysis of the coding region, the 5' UTR, and part of the promoter region in an individual affected with FBHOk did not detect any abnormalities, thereby indicating that this gene is unlikely to be implicated in the etiology of FBHOk.]. 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:9915958; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP796546.RADUnMs4TKJFPkLzelYfuNjfynGasAC9t0wDR8dRXz2_w130_publicationInfo { this: dcterms:created "2014-10-02T12:40:09+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }