@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs
> .
@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:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_head
{
this:
np:hasAssertion
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_assertion
;
np:hasProvenance
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_provenance
;
np:hasPublicationInfo
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_assertion
a
np:Assertion
.
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_provenance
a
np:Provenance
.
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNb6e2b18aafaeffa7f0cb76d6fbf5bb60
sio:SIO_000628
miriam-gene:2944
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_provenance
{
dgn-np:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_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:NP776451.RAh5mVcP-MOdo4TUPD6ZIvXOovDOIZS3_PFv2Eu3ecNhs130_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" .
}