@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk> .
@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:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_head {
  this: np:hasAssertion dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_assertion;
    np:hasProvenance dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_provenance;
    np:hasPublicationInfo dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_assertion a np:Assertion .
  
  dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_provenance a np:Provenance .
  
  dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_assertion {
  miriam-gene:54858 a ncit:C16612 .
  
  lld:C0152426 a ncit:C7057 .
  
  dgn-gda:DGN8efe06cbd2abe6b91b2aaa12667663e1 sio:SIO_000628 miriam-gene:54858, lld:C0152426;
    a sio:SIO_001121 .
}

dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_provenance {
  dgn-np:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_assertion dcterms:description
      "[The mutant genes that have been causative in disturbance of PCP in mouse models have been examined in human malformations but none of them have so far been implicated in human craniorachischisis.]. 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:19129707;
    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:NP286323.RAlkyOh-E9IPEPR95jGV1nouk-8j_8JRRAaIpW6_NcBIk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:41+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" .
}