@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A> .
@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:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_head {
   this: np:hasAssertion dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion ;
    np:hasProvenance dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance ;
    np:hasPublicationInfo dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion a np:Assertion .
  dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance a np:Provenance .
  dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion {
   miriam-gene:2158 a ncit:C16612 .
  lld:C0398623 a ncit:C7057 .
  dgn-gda:DGN2b0ad1173108aec1f02974ad6e410f53 sio:SIO_000628 miriam-gene:2158 , lld:C0398623 ;
    a sio:SIO_001122 .
}
dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_provenance {
   dgn-np:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_assertion dcterms:description "[After confirming clinically suspected thromboembolism with suitable imaging methods, pediatric patients should be screened for common gene mutations (factor V G1691A, prothrombin G20210A and MTHFR C677T genotypes), rare genetic deficiencies (protein C, protein S, antithrombin, and plasminogen), and new candidates for genetic thrombophilia causing elevated levels of lipoprotein(a), and homocysteine, and probable genetic risk factors (elevations in fibrinogen, factor IX, and factor VIIIC, and decreases in factor XII).]. 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:12172465 ;
    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:NP392648.RAdZx4S8Gr_95IXsQ83zAfRema2X2nAGcQTFZ0XkJ2C6A130_publicationInfo {
   this: dcterms:created "2015-08-25T14:41:28+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" .
}