@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg
> .
@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:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_head
{
this:
np:hasAssertion
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_assertion
;
np:hasProvenance
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_provenance
;
np:hasPublicationInfo
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_assertion
a
np:Assertion
.
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_provenance
a
np:Provenance
.
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_assertion
{
miriam-gene:26239
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNcbff4ae18988321a2842338db46143c4
sio:SIO_000628
miriam-gene:26239
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_provenance
{
dgn-np:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_assertion
dcterms:description
"[Lack of DNA polymerase eta and the attendant defect in bypass replication of pyrimidine dimers induced in DNA by ultraviolet light (UV) underlie the enhanced mutagenesis and carcinogenesis observed in xeroderma pigmentosum variant (XP-V).]. 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:12082017
;
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:NP472194.RAzxvd3Xf6RjeFajtBnpes3BN46srumivgWMOk_-kxQOg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}