@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds> .
@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:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_head {
  this: np:hasAssertion dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_assertion ;
    np:hasProvenance dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_provenance ;
    np:hasPublicationInfo dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_assertion a np:Assertion .
  dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_provenance a np:Provenance .
  dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_assertion {
  miriam-gene:1284 a ncit:C16612 .
  lld:C2931784 a ncit:C7057 .
  dgn-gda:DGN2bf5c3c209ebd1b862c305259a2a12e6 sio:SIO_000628 miriam-gene:1284 , lld:C2931784 ;
    a sio:SIO_001121 .
}
dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_provenance {
  dgn-np:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_assertion dcterms:description "[Two forms of inherited intracerebral hemorrhage (ICH) are associated with an amyloid angiopathy caused by mutations in the genes for the amyloid precursor protein or cystatin C. The purpose of this study was to determine whether patients with sporadic ICH have mutations in the amyloid precursor protein or cystatin C genes.]. 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:7945009 ;
    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:NP697687.RAtTaG6hrO8WOmRv5B2jdAv4Nq7CJu5ZU6bKsp4jgDEds130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:04+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" .
}