@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs
> .
@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:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_head
{
this:
np:hasAssertion
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_assertion
;
np:hasProvenance
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_provenance
;
np:hasPublicationInfo
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_assertion
a
np:Assertion
.
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_provenance
a
np:Provenance
.
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_assertion
{
miriam-gene:27306
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNb3f11a62a830dfca29d6198baa3bf812
sio:SIO_000628
miriam-gene:27306
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_provenance
{
dgn-np:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_assertion
dcterms:description
"[Many studies have investigated the association between glutathione S-transferase T1 (GSTT1) null genotype and risk of coronary heart disease (CHD), but the impact of GSTT1 null genotype on CHD is still unclear owing to the obvious inconsistence among those studies.]. 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:22729902
;
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:NP625911.RAbSOf00KW_bR2J-Hf_Pwkx0HvXySqTKJ49XnnstaEhAs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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
<
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}