@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s
> .
@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:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_head
{
this:
np:hasAssertion
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_assertion
;
np:hasProvenance
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_assertion
a
np:Assertion
.
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_provenance
a
np:Provenance
.
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_assertion
{
miriam-gene:9455
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNa5efc8696db78f4c98a33f3943c998be
sio:SIO_000628
miriam-gene:9455
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_provenance
{
dgn-np:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_assertion
dcterms:description
"[The action spectrum for erythema parallels the action spectrum for CPD formation in skin, and in the absence of repair, as in the genetic disease xeroderma pigmentosum (XP), skin cancer rates are dramatically increased.]. 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:15603216
;
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:NP813231.RAhjRiyXT2BZgmblp3k2KIBrvmCjJm1AJL84mBTMy8W0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}