@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20> .
@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:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_head {
  this: np:hasAssertion dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_assertion;
    np:hasProvenance dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_provenance;
    np:hasPublicationInfo dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_assertion a np:Assertion .
  
  dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_provenance a np:Provenance .
  
  dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_assertion {
  miriam-gene:4700 a ncit:C16612 .
  
  lld:C2936858 a ncit:C7057 .
  
  dgn-gda:DGNfc459033d18100a16bf9ccba6f5515be sio:SIO_000628 miriam-gene:4700, lld:C2936858;
    a sio:SIO_001121 .
}

dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_provenance {
  dgn-np:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_assertion dcterms:description
      "[In order to investigate whether these B14 positive haplotypes carry the same CYP21 mutation in the various diseases and controls, we have amplified by polymerase chain reaction (PCR) the sections of CYP21B gene which include amino acid positions 172 and 281 where typical mutations are known to occur in 21 hydroxylase deficiency.]. 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:9098443;
    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:NP712966.RAEGEIzUJDpE6ZHqJq6EGE9QkYGbLnnSQ6O5XPmc6Hx20130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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" .
}