@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M
> .
@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 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:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_head
{
this:
np:hasAssertion
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion
;
np:hasProvenance
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance
;
np:hasPublicationInfo
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion
a
np:Assertion
.
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance
a
np:Provenance
.
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN384f3c1d5d42263f0f8ca4d7c3663bc3
sio:SIO_000628
miriam-gene:2944
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_provenance
{
dgn-np:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_assertion
dct:description
"[To evaluate the occurrence of homozygous deletions of the GSTM1 and GSTT1 genes in women with sporadic breast cancer and in women without cancer and to compare breast cancer mammographic features between patients with and without these deletions.]. 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:18392488
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43174.RAjByl_7OUCNkM0PL8cUuuLJ0beXCMiMFGRWDKCUs3Z9M130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}