@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU> .
@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/v3.0.0/void/> .

dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_head {
  this: np:hasAssertion dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_assertion;
    np:hasProvenance dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_provenance;
    np:hasPublicationInfo dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_assertion a np:Assertion .
  
  dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_provenance a np:Provenance .
  
  dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_assertion {
  miriam-gene:3078 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGNf422f6b4977cf14703778bbc368d27fe sio:SIO_000628 miriam-gene:3078, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_provenance {
  dgn-np:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_assertion dcterms:description
      "[This study showed that CFH was more likely to be AMD susceptibility gene at Chr.1q31 based on the finding that the CFHR1 and CFHR3 deletion was not polymorphic in the cohort of this study, and none of the SNPs that were significantly associated with AMD in a white population in C2, CFB, and C3 genes showed a significant association with AMD.]. 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:20523265;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP447389.RA1nb48Mlv2JOaaeLsfrJqPePTxvotTJ2TdW08ADiZhyU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:02+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}