@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_head {
  this: np:hasAssertion dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion ;
    np:hasProvenance dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_provenance ;
    np:hasPublicationInfo dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion a np:Assertion .
  dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_provenance a np:Provenance .
  dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion {
  miriam-gene:57556 a ncit:C16612 .
  lld:C0004936 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_provenance {
  dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion dcterms:description "[Mice with mutations in Sema6A or the interacting genes may thus represent a highly informative model for how neurodevelopmental defects can lead to anatomical dysconnectivity, resulting, either directly or through reactive mechanisms, in dysfunction at the level of neuronal networks with associated behavioural phenotypes of relevance to psychiatric disorders.]. 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:22132072 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:20+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}