@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0> .
@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:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_head {
  this: np:hasAssertion dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_assertion;
    np:hasProvenance dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_provenance;
    np:hasPublicationInfo dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_assertion a np:Assertion .
  
  dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_provenance a np:Provenance .
  
  dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_assertion {
  miriam-gene:4781 a ncit:C16612 .
  
  lld:C0175754 a ncit:C7057 .
  
  dgn-gda:DGNf8d28a327efa731db9d946ed89bb8227 sio:SIO_000628 miriam-gene:4781, lld:C0175754;
    a sio:SIO_001121 .
}

dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_provenance {
  dgn-np:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_assertion dcterms:description
      "[It was shown that loss of NFIA results in hydrocephalus and agenesis of the corpus callosum and that NFIB deficiency leads to neurological defects and to severe lung hypoplasia, whereas Nfic knockout mice exhibit specific tooth defects.]. 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:17353270;
    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:NP451835.RAURBiJak4rBzx9uv72fyoneMDcb2nYRJQqZ7ulutsfR0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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" .
}