@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs
> .
@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:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_head
{
this:
np:hasAssertion
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_assertion
;
np:hasProvenance
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_provenance
;
np:hasPublicationInfo
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_assertion
a
np:Assertion
.
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_provenance
a
np:Provenance
.
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_assertion
{
miriam-gene:5743
a
ncit:C16612
.
lld:C0699893
a
ncit:C7057
.
dgn-gda:DGN0265c69208d0c09e7808800e51413f18
sio:SIO_000628
miriam-gene:5743
,
lld:C0699893
;
a
sio:SIO_001122
.
}
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_provenance
{
dgn-np:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_assertion
dcterms:description
"[COX-2 common variants -765G-->C and -1195A-->G appear to be associated with risk of NMSC, although in different ways in the SCC and BCC subgroups, indicating that environmental and genetic risk factors may play different roles in the outcome leading to these two phenotypes.]. 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:17578436
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP66372.RAu6TEDxoZlgmF2UthKHNsHQI8S_4VwPDx19GIyz6ohLs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}