@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_head
{
this:
np:hasAssertion
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_assertion
;
np:hasProvenance
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_assertion
a
np:Assertion
.
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_provenance
a
np:Provenance
.
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_assertion
{
miriam-gene:9455
a
ncit:C16612
.
lld:C0043346
a
ncit:C7057
.
dgn-gda:DGNe7e478a3e379d185c97af1c445ac6bb7
sio:SIO_000628
miriam-gene:9455
,
lld:C0043346
;
a
sio:SIO_001121
.
}
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_provenance
{
dgn-np:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP472930.RAwLs3g87MyFBAQ2OLzQIOlfpdwgyvtqjmBk875QJCk4Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:19+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}