@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:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_head { this: np:hasAssertion dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion; np:hasProvenance dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_provenance; np:hasPublicationInfo dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_publicationInfo; a np:Nanopublication . dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion a np:Assertion . dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_provenance a np:Provenance . dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_publicationInfo a np:PublicationInfo . } dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion { miriam-gene:157680 a ncit:C16612 . lld:C0265223 a ncit:C7057 . dgn-gda:DGNa12ed75c7874f10f1ebe3b6ffd7168d4 sio:SIO_000628 miriam-gene:157680, lld:C0265223; a sio:SIO_001121 . } dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_provenance { dgn-np:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_assertion dcterms:description "[A comparison of features among different Cohen syndrome populations with shared linkage to the COH1 locus or known COH1 gene mutations may allow for the determination of improved clinical criteria on which to suspect the diagnosis of Cohen syndrome.]. 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:15211651; 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:NP449266.RAVyVa_69K8zEJksFQ179ctfxB2CljSKg6nftow9Q7xz4130_publicationInfo { this: dcterms:created "2016-05-13T12:45:08+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" . }