@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg> .
@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:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_head {
  this: np:hasAssertion dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion;
    np:hasProvenance dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_provenance;
    np:hasPublicationInfo dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion a np:Assertion .
  
  dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_provenance a np:Provenance .
  
  dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion {
  miriam-gene:64220 a ncit:C16612 .
  
  lld:C0265783 a ncit:C7057 .
  
  dgn-gda:DGN8c8b7aec51ce3d2565cca268c72039d5 sio:SIO_000628 miriam-gene:64220, lld:C0265783;
    a sio:SIO_001121 .
}

dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_provenance {
  dgn-np:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_assertion dcterms:description
      "[Five other fetuses presenting at least one of the two major signs of clinical anophthalmia or pulmonary hypoplasia with at least one of the two associated signs of diaphragmatic closure defect or cardiopathy had no STRA6 mutations.]. 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:17503335;
    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:NP682435.RAuiRkQtWsieN9A73RW2dFPF9mzRYtTY98L6tH41u4hXg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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" .
}