@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI
> .
@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:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_head
{
this:
np:hasAssertion
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_assertion
;
np:hasProvenance
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_provenance
;
np:hasPublicationInfo
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_assertion
a
np:Assertion
.
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_provenance
a
np:Provenance
.
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_assertion
{
miriam-gene:373156
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN030b358fff7be697a86a391c0eec358c
sio:SIO_000628
miriam-gene:373156
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_provenance
{
dgn-np:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_assertion
dcterms:description
"[These findings suggest that specific single polymorphic GST genes, that is GSTM1 in the case of bladder cancer and GSTT1 in the case of prostatic carcinoma, are most relevant for the development of these urological malignancies among the general population in Central Europe.]. 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:11131031
;
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:NP271932.RATkZ44f2WHJd99LLdJOCHRGwzDQAPlUiwBUHijATOUkI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}