@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k
> .
@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:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_head
{
this:
np:hasAssertion
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_assertion
;
np:hasProvenance
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_assertion
a
np:Assertion
.
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_provenance
a
np:Provenance
.
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGN6f9d3698a48c6372fbe4154d13ff6e34
sio:SIO_000628
miriam-gene:2950
,
lld:C1458155
;
a
sio:SIO_001122
.
}
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_provenance
{
dgn-np:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_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:NP107784.RABCzc7Hcj7pYwXo2dgnMepvcWwuMEVVpe1l2jIJXCp6k130_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" .
}