@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:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_head { this: np:hasAssertion dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_assertion; np:hasProvenance dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_provenance; np:hasPublicationInfo dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_publicationInfo; a np:Nanopublication . dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_assertion a np:Assertion . dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_provenance a np:Provenance . dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_publicationInfo a np:PublicationInfo . } dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_assertion { miriam-gene:1280 a ncit:C16612 . lld:C2020284 a ncit:C7057 . dgn-gda:DGNa48372329b7217b0dd033cb5db66d92e sio:SIO_000628 miriam-gene:1280, lld:C2020284; a sio:SIO_001121 . } dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_provenance { dgn-np:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_assertion dcterms:description "[These criteria demonstrate 100% sensitivity when applied to type I Stickler syndrome patients with known COL2A1 mutations, 98% sensitivity when applied to clinically affected Stickler patients, and 86% specificity when applied to patients unaffected based on clinical and/or molecular analysis.]. 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:16152640; 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:NP512751.RAnC5sRBvlSEMt-r38gQk_d3fUV1GRlVJ-SMA0Cf0HRYY130_publicationInfo { this: dcterms:created "2016-05-13T12:45:37+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" . }