@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:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_head { this: np:hasAssertion dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_assertion; np:hasProvenance dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_provenance; np:hasPublicationInfo dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_publicationInfo; a np:Nanopublication . dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_assertion a np:Assertion . dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_provenance a np:Provenance . dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_publicationInfo a np:PublicationInfo . } dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_assertion { miriam-gene:3630 a ncit:C16612 . lld:C0011854 a ncit:C7057 . dgn-gda:DGN0a8c7921107788bc34b5e874945685d6 sio:SIO_000628 miriam-gene:3630, lld:C0011854; a sio:SIO_001121 . } dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_provenance { dgn-np:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_assertion dcterms:description "[(a) WS prevalence is not so infrequent as generally expected; (b) in our series, DM presented before 10 years in 11/12 patients and ten cases have already developed all the four peculiar manifestations of WS by 26 years; (c) 9/12 patients exhibited a homozygous frameshift/truncation mutation (Y454_L459del_fsX454), which is the one most frequently found also in patients from other Italian regions; (d) age at DM diagnosis was significantly earlier in WS group than in the patients with insulin-dependent DM of Messina district.]. 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:24497219; 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:NP1152143.RAbQ-DMJJCXKBQpGbfLvIPBqWW5hVQvhZmj9V5CNYGan0130_publicationInfo { this: dcterms:created "2016-05-13T12:50:28+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" . }