@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w
> .
@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:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_head
{
this:
np:hasAssertion
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_assertion
;
np:hasProvenance
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_assertion
a
np:Assertion
.
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_provenance
a
np:Provenance
.
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_assertion
{
miriam-gene:7508
a
ncit:C16612
.
lld:C0005695
a
ncit:C7057
.
dgn-gda:DGN44663ea64bafecb2382968fc44888af1
sio:SIO_000628
miriam-gene:7508
,
lld:C0005695
;
a
sio:SIO_001121
.
}
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_provenance
{
dgn-np:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_assertion
dcterms:description
"[Our results are consistent with the notion that the XPD (K751Q) polymorphism either individually or in combination with the XPC (K939Q) polymorphism modulates the risk of death in patients with urinary bladder neoplasms.]. 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:17438703
;
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:NP938667.RAGEIq_Vg4dXUwMkjUWCcomJCF8QibE9RWaWg2gqHhw3w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}