@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo> .
@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:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_head {
  this: np:hasAssertion dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion ;
    np:hasProvenance dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_provenance ;
    np:hasPublicationInfo dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion a np:Assertion .
  dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_provenance a np:Provenance .
  dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion {
  miriam-gene:5921 a ncit:C16612 .
  lld:C0205788 a ncit:C7057 .
  dgn-gda:DGN49c1df6bcf9a8b3b176bf9cf9cf80b2d sio:SIO_000628 miriam-gene:5921 , lld:C0205788 ;
    a sio:SIO_001121 .
}
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_provenance {
  dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion dcterms:description "[In addition to the reported venous malformation, such mutations were identified in some other subtypes of vascular anomalies, including vascular tumors (infantile hemangioma, pyogenic granuloma, and epithelioid hemangioma) and vascular malformations (capillary malformation, arteriovenous malformation, capillary lymphatic malformation, and capillary arteriovenous malformation).]. 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:21962923 ;
    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:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}