@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:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_head { this: np:hasAssertion dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_assertion; np:hasProvenance dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_provenance; np:hasPublicationInfo dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_publicationInfo; a np:Nanopublication . dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_assertion a np:Assertion . dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_provenance a np:Provenance . dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_publicationInfo a np:PublicationInfo . } dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_assertion { miriam-gene:22829 a ncit:C16612 . lld:C0004352 a ncit:C7057 . dgn-gda:DGNb60204bdd8d83b7fd1acc77debf09054 sio:SIO_000628 miriam-gene:22829, lld:C0004352; a sio:SIO_001121 . } dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_provenance { dgn-np:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_assertion dcterms:description "[The neuroligin gene family consists of five members (NLGN1 at 3q26, NLGN2 at 17p13, NLGN3 at Xq13, NLGN4 at Xp22, and NLGN4Y at Yq11), of which NLGN1 and NLGN3 are located within the best loci observed in our previous genome-wide scan for autism in the Finnish sample.]. 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:16077734; 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:NP864830.RAtUmtVEcCfgN506MYG3LRz3k_7ff1XGa_pKGL93VT970130_publicationInfo { this: dcterms:created "2015-08-25T14:46:25+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" . }