@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU> .
@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:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_head {
  this: np:hasAssertion dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion;
    np:hasProvenance dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_provenance;
    np:hasPublicationInfo dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion a np:Assertion .
  
  dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_provenance a np:Provenance .
  
  dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion {
  miriam-gene:55349 a ncit:C16612 .
  
  lld:C0018818 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_provenance {
  dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion dcterms:description
      "[The goal of our study was to identify potential pathogenic mutations in the TDGF1 gene in Chinese people with isolated CHD, particularly those with VSD, and to provide further insight into the etiology of CHD.]. 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:19853938;
    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:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}