@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:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_head { this: np:hasAssertion dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_assertion; np:hasProvenance dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_provenance; np:hasPublicationInfo dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_publicationInfo; a np:Nanopublication . dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_assertion a np:Assertion . dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_provenance a np:Provenance . dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_publicationInfo a np:PublicationInfo . } dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_assertion { miriam-gene:23380 a ncit:C16612 . lld:C3714756 a ncit:C7057 . dgn-gda:DGNa858082903d8bada9f576b5ea7868c8e sio:SIO_000628 miriam-gene:23380, lld:C3714756; a sio:SIO_001121 . } dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_provenance { dgn-np:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_assertion dcterms:description "[SrGAP3-mediated reorganisation of the actin cytoskeleton is crucial for the normal development of dendritic spines and loss of srGAP3 leads to abnormal synaptic activity and impaired cognitive behaviours in mice, which is reminiscent of an association between disrupted srGAP3 and intellectual disability in humans.]. 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:23127797; 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:NP871321.RAxd-j7cR3Eqv6EC1WNLn74O4rgI-Nl_rjI2omrN_cSJ8130_publicationInfo { this: dcterms:created "2015-08-25T14:46:30+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" . }