@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:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_head { this: np:hasAssertion dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_assertion; np:hasProvenance dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_provenance; np:hasPublicationInfo dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_publicationInfo; a np:Nanopublication . dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_assertion a np:Assertion . dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_provenance a np:Provenance . dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_publicationInfo a np:PublicationInfo . } dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_assertion { miriam-gene:3897 a ncit:C16612 . lld:C0025362 a ncit:C7057 . dgn-gda:DGN6be860ca95c7ea126085abd8cd13c092 sio:SIO_000628 miriam-gene:3897, lld:C0025362; a sio:SIO_001121 . } dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_provenance { dgn-np:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_assertion dcterms:description "[Recently, studies in the usually disparate fields of human genetics and developmental neurobiology have converged to reveal that some types of human mental retardation and brain malformations are due to mutations that affect the neural cell adhesion molecule L1.]. 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:7778187; 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:NP1321536.RAopV0Fr6vvik7vXbzKad1cV3tgtXqPPBA5W-o4SonWWE130_publicationInfo { this: dcterms:created "2016-05-13T12:51:45+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" . }