@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw
> .
@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:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_head
{
this:
np:hasAssertion
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_assertion
;
np:hasProvenance
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_assertion
a
np:Assertion
.
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_provenance
a
np:Provenance
.
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_assertion
{
miriam-gene:7508
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN870f08a6c85ef83b9bbb4aae0e3ba345
sio:SIO_000628
miriam-gene:7508
,
lld:C0025202
;
a
sio:SIO_001122
.
}
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_provenance
{
dgn-np:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_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: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:NP59339.RAfvc3JQJ7vKIiFNlqG7vTX4JQ14uNEb1u59DK_IrBjqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}