@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY> .
@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/v4.0.0/void/> .
dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_head {
  this: np:hasAssertion dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion ;
    np:hasProvenance dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance ;
    np:hasPublicationInfo dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion a np:Assertion .
  dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance a np:Provenance .
  dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion {
  miriam-gene:5654 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_provenance {
  dgn-np:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_assertion dcterms:description "[We tested whether these SNPs are associated with AMD in Israeli populations, if they underlie variable phenotype and response to therapy in neovascular AMD (NVAMD), and if HTRA1 expression in vivo is associated with its promoter variant.]. 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:19065273 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP707917.RAAfYSQdwW0Lkxbl5w1khUACuje1yweu41CsBEDHBXumY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:06+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}