@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_head {
  this: np:hasAssertion dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_assertion ;
    np:hasProvenance dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_provenance ;
    np:hasPublicationInfo dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_provenance a np:Provenance .
  dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_assertion {
  miriam-gene:1565 a ncit:C16612 .
  lld:C0010674 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_provenance {
  dgn-np:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_assertion dcterms:description "[The method was also found to accurately localise the known susceptibility variants in an empirical data set--the DeltaF508 mutation for cystic fibrosis--where the susceptibility variant is already known--and to find significant signals for association between the CYP2D6 gene and poor drug metabolism, although for this dataset the highest association score is about 60 kb from the CYP2D6 gene.]. 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:17042942 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP520220.RAjnB_Ql2sM9EObo0Vxz5nRf-LKbUquoBEra0-rY3EHW8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:09+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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