@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg> .
@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:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_head {
   this: np:hasAssertion dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_assertion ;
    np:hasProvenance dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_provenance ;
    np:hasPublicationInfo dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_assertion a np:Assertion .
  dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_provenance a np:Provenance .
  dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_assertion {
   miriam-gene:5340 a ncit:C16612 .
  lld:C0398623 a ncit:C7057 .
  dgn-gda:DGNafab74b583b9758a513c45ba357be75b sio:SIO_000628 miriam-gene:5340 , lld:C0398623 ;
    a sio:SIO_001122 .
}
dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_provenance {
   dgn-np:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_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:NP630449.RAiaFNDaO4RORJ-Uv46QgvpoE0PZ2GH9SntFKjmOxCqbg130_publicationInfo {
   this: dcterms:created "2015-08-25T14:43:57+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" .
}