@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc> .
@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/v4.0.0/void/> .

dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_head {
  this: np:hasAssertion dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_assertion;
    np:hasProvenance dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_provenance;
    np:hasPublicationInfo dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_assertion a np:Assertion .
  
  dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_provenance a np:Provenance .
  
  dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_assertion {
  miriam-gene:6473 a ncit:C16612 .
  
  lld:C0041408 a ncit:C7057 .
  
  dgn-gda:DGNd438da01cd24f723e1257883a8128939 sio:SIO_000628 miriam-gene:6473, lld:C0041408;
    a sio:SIO_001121 .
}

dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_provenance {
  dgn-np:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_assertion dcterms:description
      "[Although clinical features of Turner syndrome have primarily been explained by the dosage effects of SHOX (short stature homeobox-containing gene) and the putative lymphogenic gene together with chromosomal effects leading to nonspecific features, several matters remain to be determined, including modifying factors for the effects of SHOX haploinsufficiency, chromosomal location of the lymphogenic gene, and genetic factors for miscellaneous features such as multiple pigmented nevi.]. 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:11701728;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP335823.RAXa31Xv96c-QIrJkbstAjRvIoeexBSxmdF6A2aapuMkc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:17+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}