@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0> .
@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:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_head {
  this: np:hasAssertion dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_assertion;
    np:hasProvenance dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_provenance;
    np:hasPublicationInfo dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_assertion a np:Assertion .
  
  dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_provenance a np:Provenance .
  
  dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
  dgn-gda:DGN8a0e44dcc64c1ed6875f0062ca8fa6dc sio:SIO_000628 miriam-gene:2952, lld:C0036421;
    a sio:SIO_001121 .
}

dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_provenance {
  dgn-np:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_assertion dcterms:description
      "[The data show that while M1 and T1 null genotypes were not significantly increased in SSc compared to ethnically matched controls, their frequencies (especially T1 nulls) were significantly higher among SSc patients with hypertension and pulmonary involvement.]. 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:11477481;
    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:NP440551.RA6mRavyp93eJZHWJB3aehPhL7mEfBf1Q-_BuQaHSMMY0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:57+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" .
}