@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw> .
@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 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:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_head {
   this: np:hasAssertion dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_assertion ;
    np:hasProvenance dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_provenance ;
    np:hasPublicationInfo dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_assertion a np:Assertion .
  dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_provenance a np:Provenance .
  dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_assertion {
   miriam-gene:659 a ncit:C16612 .
  lld:C2973725 a ncit:C7057 .
  dgn-gda:DGNf07ddb873dc542c5f500247f4c1ced70 sio:SIO_000628 miriam-gene:659 , lld:C2973725 ;
    a sio:SIO_001122 .
}
dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_provenance {
   dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_assertion dct:description "[BMPR2 was examined for mutations in 33 unrelated patients with sporadic PAH, and in two sisters with PAH, all of whom had taken fenfluramine derivatives, as well as in 130 normal controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_curated ;
    sio:SIO_000772 miriam-pubmed:12358323 ;
    prov:wasDerivedFrom dgn-void:uniprot-20130724 ;
    prov:wasGeneratedBy eco:ECO_0000218 .
  dgn-void:source_evidence_curated a eco:ECO_0000205 ;
    rdfs:comment "Gene-disease associations manually curated."@en ;
    rdfs:label "DisGeNET evidence - CURATED"@en .
  dgn-void:uniprot-20130724 pav:importedOn "2013-07-24"^^xsd:date .
}
dgn-np:NP758.RATHmpJVhw6oqBPWiwaTd8kdoiic_rYvz4vzxbCnQrCmw130_publicationInfo {
   this: dct:created "2014-10-02T12:31:58+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}