@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4
> .
@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:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_head
{
this:
np:hasAssertion
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_assertion
;
np:hasProvenance
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_assertion
a
np:Assertion
.
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_provenance
a
np:Provenance
.
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_assertion
{
miriam-gene:7508
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN975d555e5749379edf0d2337f02b6c73
sio:SIO_000628
miriam-gene:7508
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_provenance
{
dgn-np:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_assertion
dcterms:description
"[The results indicated that there was a significant modifying effect on the association between genotype XPC PAT and exon 15 polymorphism and PCa risk which was further confirmed by diplotype analysis of XPC PAT and exon 15 in north Indian population.]. 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:22382185
;
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:NP317449.RAR8KN5S41cZ0ieMJ_FEN3vz7X1VZgv1Fc8ePZu8hCrh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}