@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk> .
@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:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_head {
  this: np:hasAssertion dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion;
    np:hasProvenance dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_provenance;
    np:hasPublicationInfo dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion a np:Assertion .
  
  dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_provenance a np:Provenance .
  
  dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion {
  miriam-gene:1357 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGN5ce5735174c5c70801cba1a6eeeac0ed sio:SIO_000628 miriam-gene:1357, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_provenance {
  dgn-np:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_assertion dcterms:description
      "[We have analyzed, using the mixed model, the whole sample of nonsyndromic CP, including isolated (i.e., without other anomalies) CP (CPI) and CP associated with at least one other anomaly (CPA), for which a diagnosis of malformation syndrome was not possible.]. 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:9254850;
    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:NP692412.RAYSVmnIa62fS4QlAsNv5a1mr0yF_ot6HpB5Aw8OIMeuk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}