@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU> .
@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 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:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_head {
  this: np:hasAssertion dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion;
    np:hasProvenance dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_provenance;
    np:hasPublicationInfo dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion a np:Assertion .
  
  dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_provenance a np:Provenance .
  
  dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion {
  miriam-gene:875 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN8c1bdedec8198cbd4700109dc9236232 sio:SIO_000628 miriam-gene:875, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_provenance {
  dgn-np:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_assertion dc:description
      "[In order to clarify whether cystathionine beta-synthase (CBS) could differentiate groups of patients with various vascular diagnosis, CBS was studied in cultured human skin fibroblasts from 99 human subjects diagnosed as homozygotes or heterozygotes for CBS deficiency or suffering from atherosclerotic vascular disease or Down's syndrome (prone to less atherosclerosis).]. 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:1385957;
    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:NP369448.RAC1IXBs6kDqrFCNTJxmeDzC-D1xvsq1RZGzGKxQkLguU130_publicationInfo {
  this: dc:created "2014-10-02T12:35:36+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}