@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k> .
@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:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_head {
  this: np:hasAssertion dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_assertion;
    np:hasProvenance dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_provenance;
    np:hasPublicationInfo dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_assertion a np:Assertion .
  
  dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_provenance a np:Provenance .
  
  dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_assertion {
  miriam-gene:78987 a ncit:C16612 .
  
  lld:C0037221 a ncit:C7057 .
  
  dgn-gda:DGNccd4391c78997838ece73ad98000b943 sio:SIO_000628 miriam-gene:78987, lld:C0037221;
    a sio:SIO_001121 .
}

dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_provenance {
  dgn-np:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_assertion dcterms:description
      "[CRELD1 is the first human gene to be implicated in the pathogenesis of isolated AVSD and AVSD in the context of heterotaxy, which provides an important step in unraveling the pathogenesis of AVSD.]. 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:12632326;
    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:NP640473.RAwnqjChN4i5ig7nInLp1Do3zqB_1AA1uwlfeM6oodP9k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}