@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_assertion
;
np:hasProvenance
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_provenance
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np:hasPublicationInfo
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_assertion
a
np:Assertion
.
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_provenance
a
np:Provenance
.
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:27352
a
ncit:C16612
.
lld:C0013146
a
ncit:C7057
.
dgn-gda:DGN4f28c6b6b766a1815521d48fbf456585
sio:SIO_000628
miriam-gene:27352
,
lld:C0013146
;
a
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.
}
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_provenance
{
dgn-np:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_assertion
dcterms:description
"[To clarify the potential role and mechanisms of genetic polymorphisms of GSTM1 and T1 in susceptibility to MAP abuse in the Japanese population, we investigated GSTM1 and T1 polymorphisms in subjects with diagnosed MAP-related disorders and in control groups.]. 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:19254865
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
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:NP712224.RAAw8UrY1ktOqhIb8X0C_HEZY_jp7pNqvhQpacA0hDvBY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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:disgenetrdf
;
pav:authoredBy
<
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> , <
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> , <
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
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dgn-void:disgenetrdf
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"v2.1.0" .
}