@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY
> .
@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:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_head
{
this:
np:hasAssertion
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_assertion
;
np:hasProvenance
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_provenance
;
np:hasPublicationInfo
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_assertion
a
np:Assertion
.
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_provenance
a
np:Provenance
.
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_assertion
{
miriam-gene:728340
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGNc8e96683f9a23c8ab83d1a5ef45d5343
sio:SIO_000628
miriam-gene:728340
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_provenance
{
dgn-np:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_assertion
dcterms:description
"[Moreover, mutations in the TFIIH subunits XPB and XPD found in Cockayne syndrome impair the interaction of TFIIH with the rDNA, but do not influence initiation complex formation or promoter escape of RNA polymerase I, but preclude the productivity of the enzyme by reducing transcription elongation in vivo and in vitro.]. 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:21965540
;
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:NP217789.RApxD09Q-5hOZ_82wo3zVlROEAFME4xIKBPt1H-ZuwuQY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}