@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY> .
@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/v4.0.0/void/> .

dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_head {
  this: np:hasAssertion dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion;
    np:hasProvenance dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_provenance;
    np:hasPublicationInfo dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion a np:Assertion .
  
  dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_provenance a np:Provenance .
  
  dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion {
  miriam-gene:1351 a ncit:C16612 .
  
  lld:C0019069 a ncit:C7057 .
  
  dgn-gda:DGN63bd43edda926281278601cd829b44a9 sio:SIO_000628 miriam-gene:1351, lld:C0019069;
    a sio:SIO_001121 .
}

dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_provenance {
  dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion dcterms:description
      "[The identification of fetal genetic disease has, for the most part, relied on examination of an end product, such as analysis of factor VIII levels obtained from cord blood in fetuses at risk for hemophilia.]. 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:7858372;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:46+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}