@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA
> .
@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:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_head
{
this:
np:hasAssertion
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_assertion
;
np:hasProvenance
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_provenance
;
np:hasPublicationInfo
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_assertion
a
np:Assertion
.
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_provenance
a
np:Provenance
.
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0020676
a
ncit:C7057
.
dgn-gda:DGN7a3c1c3b564c8954a8599088d66f97dc
sio:SIO_000628
miriam-gene:2944
,
lld:C0020676
;
a
sio:SIO_001121
.
}
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_provenance
{
dgn-np:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_assertion
dcterms:description
"[Our results showed that the GSTM1 and GSTT1 null genotypes were not associated with any incidence of endocrine dysfunction (including diabetes mellitus, hypogonadism, hypothyroidism, and growth hormone deficiency), liver function, or impaired left ventricular ejection fraction (LVEF).]. 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:16798650
;
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:NP330316.RA1qwTWf0P3PStez4D0vRsZ0oRqHymhSPSu_oCEVwzYHA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}