@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo> .
@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:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_head {
  this: np:hasAssertion dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion;
    np:hasProvenance dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_provenance;
    np:hasPublicationInfo dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion a np:Assertion .
  
  dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_provenance a np:Provenance .
  
  dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion {
  miriam-gene:29974 a ncit:C16612 .
  
  lld:C0000768 a ncit:C7057 .
  
  dgn-gda:DGNf9bdb197204b1aa0d16347606f58d18a sio:SIO_000628 miriam-gene:29974, lld:C0000768;
    a sio:SIO_001121 .
}

dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_provenance {
  dgn-np:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_assertion dcterms:description
      "[The present report describes a case with cardiofacial syndrome and ACF associated other congenital anomalies, and provides criteria for differentiating absence of the depressor anguli oris muscle (DAOM) from palsy of the seventh cranial nerve and its central connections.]. 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:8741317;
    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:NP229421.RADvCeyBtdxc_eiYYQ8LbJsNQBUlEqwte3zwj8mO6IkIo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:08+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" .
}