@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM
> .
@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:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_head
{
this:
np:hasAssertion
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_assertion
;
np:hasProvenance
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_provenance
;
np:hasPublicationInfo
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_assertion
a
np:Assertion
.
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_provenance
a
np:Provenance
.
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_assertion
{
miriam-gene:847
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGN53afeb53357151ff598d0c66fcae848b
sio:SIO_000628
miriam-gene:847
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_provenance
{
dgn-np:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_assertion
dcterms:description
"[In several fibroblast cell lines from patients suffering from Cockayne Syndrome expression of UV damaged CAT gene was restored significantly less than in normal fibroblasts, indicating that Cockayne Syndrome is associated with a UV repair defect.]. 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:3956512
;
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:NP911533.RACnABbmWZOJOQl-GPBSPd_UbiZp8AtpE5rO5FXTYoSiM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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: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" .
}