@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A> .
@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:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_head {
  this: np:hasAssertion dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_assertion;
    np:hasProvenance dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_provenance;
    np:hasPublicationInfo dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_assertion a np:Assertion .
  
  dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_provenance a np:Provenance .
  
  dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_assertion {
  miriam-gene:3075 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGNfb228ad75fe767c2e1024374fd8b71e7 sio:SIO_000628 miriam-gene:3075, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_provenance {
  dgn-np:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_assertion dcterms:description
      "[We identified a sample of patients with neovascular AMD, that in previous studies had been shown to be at elevated risk for the disease through environmental factors such as cigarette smoking and genetic variants including the complement factor H gene (CFH) on chromosome 1q25 and variants in the ARMS2/HtrA serine peptidase 1 (HTRA1) gene(s) on chromosome 10q26.]. 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:21682878;
    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:NP902909.RALKwTqt9PHEHfBEhj9m4v_owJ3sdjnPIpfmH5qLD_b-A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:33+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:disgenetv3.0rdf;
    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" .
}