@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_assertion
a
np:Assertion
.
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_provenance
a
np:Provenance
.
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN24aa5191a821a167ea58b6921f8c06f3
sio:SIO_000628
miriam-gene:2950
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_provenance
{
dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_assertion
dcterms:description
"[Our results suggest that the variants in low penetrance genes such as GSTM1, GSTT1 and GSTP1 are associated with an increased breast cancer risk thereby suggesting their contribution in the etiology of breast cancer.]. 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:18574688
;
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 .
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dgn-np:NP678338.RAbEmU9FUh2NghPhyj5DN7VKkrFP2_vy-J_7VFWU27rqo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:52+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
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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" .
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"v4.0.0" .
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