@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0> .
@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:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_head {
  this: np:hasAssertion dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_assertion;
    np:hasProvenance dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_provenance;
    np:hasPublicationInfo dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_assertion a np:Assertion .
  
  dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_provenance a np:Provenance .
  
  dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_assertion {
  miriam-gene:170474 a ncit:C16612 .
  
  lld:C0220681 a ncit:C7057 .
  
  dgn-gda:DGNa76f7cdb45359a4e39dfdca634e0c00f sio:SIO_000628 miriam-gene:170474, lld:C0220681;
    a sio:SIO_001121 .
}

dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_provenance {
  dgn-np:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_assertion dcterms:description
      "[We describe a patient presenting with developmental delay, patent foramen ovale, moderate short QT interval, and facial dysmorphism including left microtia, preauricular tag and pit, wide left corner of the mouth, and left hemifacial microsomia, fitting with the oculoauriculovertebral spectrum.]. 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:19733267;
    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:NP776009.RAEfQNUBV0jpz_CEIfGsxXJsmbacHUPMNsXL-i9rAv4g0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:50+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" .
}