@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA
> .
@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:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_head
{
this:
np:hasAssertion
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_assertion
;
np:hasProvenance
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_provenance
;
np:hasPublicationInfo
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_assertion
a
np:Assertion
.
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_provenance
a
np:Provenance
.
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0020676
a
ncit:C7057
.
dgn-gda:DGNb970a99b4d27f3ca3a19836048fc4268
sio:SIO_000628
miriam-gene:2952
,
lld:C0020676
;
a
sio:SIO_001121
.
}
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_provenance
{
dgn-np:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_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:NP255447.RAs4epWtfvj7InFQ6y4F2raULJ1tTio1kCFx0lAVay8MA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}