@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8
> .
@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:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_head
{
this:
np:hasAssertion
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_assertion
;
np:hasProvenance
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_provenance
;
np:hasPublicationInfo
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_assertion
a
np:Assertion
.
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_provenance
a
np:Provenance
.
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_assertion
{
miriam-gene:7508
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNff9f9317a4b4a5d6160856df4fd8a361
sio:SIO_000628
miriam-gene:7508
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_provenance
{
dgn-np:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_assertion
dcterms:description
"[The results of our case-control study support the hypothesis that the intron 9 PAT+, intron 11 -6A and exon 15 2920C haplotype may contribute to the risk of developing cutaneous melanoma by increasing the rate of an alternatively spliced XPC mRNA isoform that skips exon 12 and leads to reduced DNA repair.]. 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:15731165
;
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:NP661264.RAbhfR8C3z2ZvF-2F9bSrSlCC4yM-IrHztXNe5PYQFOs8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}