@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo> .
@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:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_head {
  this: np:hasAssertion dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_assertion;
    np:hasProvenance dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_provenance;
    np:hasPublicationInfo dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_assertion a np:Assertion .
  
  dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_provenance a np:Provenance .
  
  dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_assertion {
  miriam-gene:6473 a ncit:C16612 .
  
  lld:C1845118 a ncit:C7057 .
  
  dgn-gda:DGN5ae472d874337fcb07458a76183745b4 sio:SIO_000628 miriam-gene:6473, lld:C1845118;
    a sio:SIO_001121 .
}

dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_provenance {
  dgn-np:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_assertion dcterms:description
      "[The high frequency of SHOX anomalies in the ISS group can be explained by the large proportion of boys in this group, reflecting the difficulty in diagnosing dyschondrosteosis in young boys.]. 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:16597678;
    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:NP336773.RAxQ2hb4UFSaPGVbahOpAnS6NTfNglMPMy8T5VNLF7czo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:18+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" .
}