@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_assertion
;
np:hasProvenance
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_provenance
;
np:hasPublicationInfo
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_assertion
a
np:Assertion
.
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_provenance
a
np:Provenance
.
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2952
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN8a2d5aba42a314e06bbf51aa998d1b81
sio:SIO_000628
miriam-gene:2952
,
lld:C1527249
;
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.
}
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_provenance
{
dgn-np:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_assertion
dcterms:description
"[Because GSTM1 and GSTT1 gene deficiencies may act as risk modifiers for colorectal cancer risk, we investigated the relationship between genetic polymorphism in these genes and colorectal cancer risk in Egyptians.]. 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:10424787
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP245747.RAQ8mTRZ2Mg72BNQC4C5-c03fNhxqAPIy-ofQ2PwlQKKk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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
<
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> , <
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" .
}