@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I> .
@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:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_head {
  this: np:hasAssertion dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_assertion;
    np:hasProvenance dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_provenance;
    np:hasPublicationInfo dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_assertion a np:Assertion .
  
  dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_provenance a np:Provenance .
  
  dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C2673195 a ncit:C7057 .
  
  dgn-gda:DGN587c3cd0c83052cd221ef1e22c0cb199 sio:SIO_000628 miriam-gene:7428, lld:C2673195;
    a sio:SIO_001121 .
}

dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_provenance {
  dgn-np:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_assertion dcterms:description
      "[The maps indicated that mutations affecting major ligand-binding sites, for example, for Von Hippel Lindau (VHL) protein in the α1 chain or integrins in the α5 chain, resulted in distinctive phenotypes (Hereditary Angiopathy, Nephropathy, Aneurysms, and muscle Cramps [HANAC] syndrome, and early-onset Alport syndrome, respectively).]. 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:21280145;
    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:NP670836.RAJPbPc6eRdyGCCiKMtIn2CRCdF1WY8Z7Ba8zPSHWYH_I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:45+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" .
}