@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0
> .
@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:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_head
{
this:
np:hasAssertion
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_assertion
;
np:hasProvenance
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_provenance
;
np:hasPublicationInfo
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_assertion
a
np:Assertion
.
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_provenance
a
np:Provenance
.
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_assertion
{
miriam-gene:9455
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGN464516aa1961f3f27c82ea57497149ec
sio:SIO_000628
miriam-gene:9455
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_provenance
{
dgn-np:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_assertion
dcterms:description
"[Transfection of the human CSB gene into UV61 restores the normal repair pattern (CPD removal in only the transcribed strand), demonstrating that the DNA repair defect in UV61 is homologous to that in Cockayne's syndrome (complementation group B) cells.]. 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:8811084
;
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:NP409908.RAlvm-hVvcB6EmphbO9QQSRIKZ-X9taHyPq83jPN1vWp0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}