@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI
> .
@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:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_head
{
this:
np:hasAssertion
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_assertion
;
np:hasProvenance
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_provenance
;
np:hasPublicationInfo
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_assertion
a
np:Assertion
.
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_provenance
a
np:Provenance
.
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNa3a68aeb3776b177ae9cced95cf79d71
sio:SIO_000628
miriam-gene:2944
,
lld:C1458155
;
a
sio:SIO_001122
.
}
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_provenance
{
dgn-np:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_assertion
dcterms:description
"[The only significant association between increased risk of breast cancer development and GSTs polymorphisms is found when GSTT1 null, GSTM1 null and the presence of valine in GSTP1 in codon 105 are combined.]. 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:18521819
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP107644.RAeFdn7XfxiX9R7cJokXZBmRuEDLNkAOz-yr6FfxKS3tI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:55+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" .
}