@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg
> .
@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/v4.0.0/void/
> .
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_head
{
this:
np:hasAssertion
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_assertion
;
np:hasProvenance
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_provenance
;
np:hasPublicationInfo
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_assertion
a
np:Assertion
.
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_provenance
a
np:Provenance
.
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNf2b35c03c6d6774a240168c7fe26fb5b
sio:SIO_000628
miriam-gene:2952
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_provenance
{
dgn-np:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_assertion
dcterms:description
"[This study showed no evidence for altered risk of breast cancer for individuals with the GSTT1 and GSTM1 deletion variants, but did report that the GSTP1 Ile105Val (rs1695) variant was associated with increased breast cancer risk in carriers.]. 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:19921428
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP776457.RA7qZZfts6J5dw3ZYpthRojl3fm09xqp9MdEyfQ3Sh7Hg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:37+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}