@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_head {
  this: np:hasAssertion dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion;
    np:hasProvenance dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_provenance;
    np:hasPublicationInfo dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion a np:Assertion .
  
  dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_provenance a np:Provenance .
  
  dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion {
  miriam-gene:6926 a ncit:C16612 .
  
  lld:C1866994 a ncit:C7057 .
  
  dgn-gda:DGN92676a8a32e9bfce0fdee4a7b52d2e52 sio:SIO_000628 miriam-gene:6926, lld:C1866994;
    a sio:SIO_001121 .
}

dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_provenance {
  dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion dcterms:description
      "[Ulnar mammary syndrome (UMS), an autosomal dominant disorder caused by mutations in TBX3, underscores the importance of TBX3 in human breast development, while abnormal mammary gland development in Tbx2 or Tbx3 mutant mice provides models for experimental investigation.]. 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:23624936;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:57+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}