@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_head
{
this:
np:hasAssertion
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_assertion
a
np:Assertion
.
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_provenance
a
np:Provenance
.
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_assertion
{
miriam-gene:373156
a
ncit:C16612
.
lld:C0040136
a
ncit:C7057
.
dgn-gda:DGN0a8c33322fa6e70d691c72a99e54bd9f
sio:SIO_000628
miriam-gene:373156
,
lld:C0040136
;
a
sio:SIO_001121
.
}
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_provenance
{
dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_assertion
dcterms:description
"[The rationale for our study was that according to the important roles of GST enzymes in cells and association of GST null genotypes with many types of tumors, inactivating polymorphisms may be genetic susceptibility factors in the etiology of oxyphilic thyroid tumors characterized by mitochondrial dysfunction, increased ROS production and resistance to chemio- and radio-therapy.]. 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:16427734
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP988186.RAMd1OpngVC0lmNS0XEs3qZoo4jfZDj1xQMaIBYGJvJyE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:45+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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pav:version
"v3.0.0" .
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