@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:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_head { this: np:hasAssertion dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_assertion; np:hasProvenance dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_provenance; np:hasPublicationInfo dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_publicationInfo; a np:Nanopublication . dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_assertion a np:Assertion . dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_provenance a np:Provenance . dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_publicationInfo a np:PublicationInfo . } dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_assertion { miriam-gene:1203 a ncit:C16612 . lld:C0008073 a ncit:C7057 . dgn-gda:DGN86feba069800bd953da8ecba5d8b84a5 sio:SIO_000628 miriam-gene:1203, lld:C0008073; a sio:SIO_001121 . } dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_provenance { dgn-np:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_assertion dcterms:description "[Material includes 159 probands with NCL (37 CLNI, 72 classical CLN2, 10 variant LINCL, and 40 CLN3) collected at the New York State Institute for Basic Research in Developmental Disabilities (IBR) as well as a comprehensive review of the literature.]. 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:11332767; 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:NP316158.RAa7gtgCo0D7XxJaIB07GsJGLvSfStreRUYXEB5pwry14130_publicationInfo { this: dcterms:created "2015-08-25T14:40:41+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" . }