@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU
> .
@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:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_head
{
this:
np:hasAssertion
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_assertion
;
np:hasProvenance
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_provenance
;
np:hasPublicationInfo
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_assertion
a
np:Assertion
.
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_provenance
a
np:Provenance
.
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_assertion
{
miriam-gene:9455
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGN7b2a415489a63f83d9c0cfbfaddea9a3
sio:SIO_000628
miriam-gene:9455
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_provenance
{
dgn-np:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_assertion
dcterms:description
"[Removal of ultraviolet light induced cyclobutane pyrimidine dimers (CPD) from active and inactive genes was analyzed in cells derived from patients suffering from the hereditary disease Cockayne's syndrome (CS) using strand specific probes.]. 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:8290349
;
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:NP781885.RAGfPz-060kTvxkH0NIfubzok0fQoX8PDem1PhdjabXqU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}