@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos
> .
@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:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_head
{
this:
np:hasAssertion
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_assertion
;
np:hasProvenance
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_provenance
;
np:hasPublicationInfo
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_assertion
a
np:Assertion
.
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_provenance
a
np:Provenance
.
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0023531
a
ncit:C7057
.
dgn-gda:DGN84a3687d38dbc8fa0a95d4958908668a
sio:SIO_000628
miriam-gene:7515
,
lld:C0023531
;
a
sio:SIO_001121
.
}
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_provenance
{
dgn-np:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_assertion
dcterms:description
"[Therefore, the presence of variant haplotypes on XRCC1 and two risk genotypes, one on each of two loci, GSTM3 and XRCC1, could be useful to determine the leukoplakias that might progress to cancer in a group of patients.]. 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:16172217
;
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:NP427453.RAg639Iefxnela8euHo1nsHPOxhR1N7_28ibu8G-vumos130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}