@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0> .
@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:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_head {
  this: np:hasAssertion dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion;
    np:hasProvenance dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_provenance;
    np:hasPublicationInfo dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion a np:Assertion .
  
  dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_provenance a np:Provenance .
  
  dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion {
  miriam-gene:2296 a ncit:C16612 .
  
  lld:C0018817 a ncit:C7057 .
  
  dgn-gda:DGN5e0f2299eab808a9007bd834b8f8cb43 sio:SIO_000628 miriam-gene:2296, lld:C0018817;
    a sio:SIO_001121 .
}

dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_provenance {
  dgn-np:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_assertion dcterms:description
      "[This is further supported by our studies showing that mutations in the FKHL7 gene were associated with defects in the anterior segment of the eye as well as atrial septal defects or mitral valve 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:10474162;
    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:NP289613.RAZzxQJjDB1vf8NYnCoffIXxFtOR-ogbZsfoNyj7KK8m0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}