@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk
> .
@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/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_assertion
a
np:Assertion
.
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_provenance
a
np:Provenance
.
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGN188a987f43359eb5b66bd484e2ed7bbd
sio:SIO_000628
miriam-gene:10
,
lld:C0546837
;
a
sio:SIO_001122
.
}
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_provenance
{
dgn-np:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_assertion
dcterms:description
"[These variants could therefore be associated with high cancer susceptibility. In addition, the high proportion of NAT2 fast alleles may partially explain the high tuberculosis prevalence in South Africans, due to reduced isoniazid efficacy in the presen]. 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:12747608
;
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:NP79734.RAnX77O15vc0FU_1oeyg_MewtTDw5emdpkYo9xY87uljk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:24+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
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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
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}