@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco
> .
@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 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:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_head
{
this:
np:hasAssertion
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion
;
np:hasProvenance
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_provenance
;
np:hasPublicationInfo
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion
a
np:Assertion
.
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_provenance
a
np:Provenance
.
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN9a2dc28ef48b64ffbe7cf5a03c06aa1d
sio:SIO_000628
miriam-gene:7376
,
lld:C0242379
;
a
sio:SIO_001121
.
}
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_provenance
{
dgn-np:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_assertion
dct:description
"[Mutations in the DDB2 gene can cause a repair-deficiency syndrome xeroderma pigmentosum group E. Because tobacco carcinogens can cause DNA damage that is repaired by NER and suboptimal NER capacity is reported to be associated with lung cancer risk, we hypothesized that common variants in the DDB2 gene are associated with lung cancer risk.]. 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:16522664
;
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:NP362563.RAB18cPBJb_Qda4Uw_WVXICjcVsQ_fHFzxX7vZU6bglco130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:32+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}