@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ> .
@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:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_head {
   this: np:hasAssertion dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_assertion ;
    np:hasProvenance dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_provenance ;
    np:hasPublicationInfo dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_assertion a np:Assertion .
  dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_provenance a np:Provenance .
  dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_assertion {
   miriam-gene:2158 a ncit:C16612 .
  lld:C0472801 a ncit:C7057 .
  dgn-gda:DGNd28f897bfcdb0839518365708b371830 sio:SIO_000628 miriam-gene:2158 , lld:C0472801 ;
    a sio:SIO_001121 .
}
dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_provenance {
   dgn-np:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_assertion dcterms:description "[The approach for hemophilia A carrier detection includes tests for BclI, XbaI, and TaqI polymorphic sites for introns 18 and 22 and the extragenic locus St 14, respectively, whereas for hemophilia B, tests include detection of TaqI, DdeI, and HhaI polymorphic sites for introns 4 and 1, and the 3' flanking region of the factor IX gene, respectively.]. 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:9092680 ;
    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:NP698942.RAzw6mIKW2UOePV7NM7nEk3OSCTRbouCh25uuQp2P1iZQ130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:05+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" .
}