@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs
> .
@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:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_head
{
this:
np:hasAssertion
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_assertion
;
np:hasProvenance
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_assertion
a
np:Assertion
.
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_provenance
a
np:Provenance
.
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_assertion
{
miriam-gene:1362
a
ncit:C16612
.
lld:C0041834
a
ncit:C7057
.
dgn-gda:DGN66242dcb9d5f844aca270b3a3fb67c4f
sio:SIO_000628
miriam-gene:1362
,
lld:C0041834
;
a
sio:SIO_001121
.
}
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_provenance
{
dgn-np:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_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:NP549421.RADJC1MWrxfWrz_Q43ZPHKuFHos2Q5cJUB--VNgqMxfvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}