@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0> .
@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:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_head {
   this: np:hasAssertion dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_assertion ;
    np:hasProvenance dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_provenance ;
    np:hasPublicationInfo dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_assertion a np:Assertion .
  dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_provenance a np:Provenance .
  dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_assertion {
   miriam-gene:8546 a ncit:C16612 .
  lld:C0333007 a ncit:C7057 .
  dgn-gda:DGN2c1d6983ae3981f5d16b305b92a930af sio:SIO_000628 miriam-gene:8546 , lld:C0333007 ;
    a sio:SIO_001121 .
}
dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_provenance {
   dgn-np:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_assertion dcterms:description "[Thirty-one single nucleotide polymorphisms (SNPs) in genes that had been mainly associated with congenital pigmentation syndromes (ADTB3A, ATRN, CHS1, EDNRB, HPS, KIT, MGRN1, MITF, MLANA, MYO5A, MYO7A, OA1, OCA2, PAX3 and SOX10) were selected.]. 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:19320733 ;
    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:NP798106.RAjiCFMHbQvFdeb-5QchglNeJdoLCsJ08lWMiFPvbaKo0130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:43+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" .
}