@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw> .
@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:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_head {
  this: np:hasAssertion dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_assertion ;
    np:hasProvenance dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_provenance ;
    np:hasPublicationInfo dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_assertion a np:Assertion .
  dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_provenance a np:Provenance .
  dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_assertion {
  miriam-gene:6319 a ncit:C16612 .
  lld:C0002895 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_provenance {
  dgn-np:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_assertion dcterms:description "[If future carefully controlled studies confirm the hypothesis of influence of hypermelanotic or hypomelanotic skin status of the individual patients on severity in phenotypic expression of homozygous SCD, genetic and pharmacological interventions aimed at regulation of melanin production may play a role in alleviating the severity in phenotypic expression of SCD in affected patients.]. 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:21288648 ;
    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:NP682180.RA565QWSmlAloJ_oxQUDWW5bPhBalvfZrOWqo5P8UwLkw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:31+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> ;
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    pav:version "v3.0.0.0" .
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}