@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA
> .
@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:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_assertion
;
np:hasProvenance
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_provenance
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np:hasPublicationInfo
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_assertion
a
np:Assertion
.
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_provenance
a
np:Provenance
.
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2952
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGN0c73015a3b41cc983194e1690eed4324
sio:SIO_000628
miriam-gene:2952
,
lld:C0029463
;
a
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.
}
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_provenance
{
dgn-np:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_assertion
dcterms:description
"[This study aims to investigate the genotype frequencies of GSTM1, GSTT1 and GSTM3 genes in 80 osteosarcoma patients and 160 normal control participants, and also the influence of these polymorphisms in the clinical outcome of osteosarcoma patients.]. 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:20577141
;
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:NP172934.RATFx3ifTEYlyPj_Q5u9WGbLsRkAOq2USIgt0IWTBUnqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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
<
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> ;
pav:version
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dgn-void:disgenetrdf
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"v2.1.0" .
}