@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI> .
@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:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_head {
  this: np:hasAssertion dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_assertion ;
    np:hasProvenance dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_provenance ;
    np:hasPublicationInfo dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_assertion a np:Assertion .
  dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_provenance a np:Provenance .
  dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_assertion {
  miriam-gene:387715 a ncit:C16612 .
  lld:C0008521 a ncit:C7057 .
  dgn-gda:DGN06a8ac343dd63c7f23e7f26e2420faf5 sio:SIO_000628 miriam-gene:387715 , lld:C0008521 ;
    a sio:SIO_001122 .
}
dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_provenance {
  dgn-np:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_assertion dcterms:description "[The association pattern and haplotype estimation in the ARMS2/HTRA1 region of Japanese patients with PCV were very similar to those of Japanese patients with typical nAMD. The polymorphisms responsible for nAMD and PCV may be located in this region or in ]. 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:21191724 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP98205.RAcoTRtmhxnxOz57X9NV_FVqB-xPxVdue81V0qwH4uRHI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:34+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" .
}