@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU
> .
@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:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_head
{
this:
np:hasAssertion
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_assertion
;
np:hasProvenance
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_assertion
a
np:Assertion
.
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_provenance
a
np:Provenance
.
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_assertion
{
miriam-gene:2072
a
ncit:C16612
.
lld:C0009207
a
ncit:C7057
.
dgn-gda:DGN994fcc5e6287344bfc0e7c1a590e6daf
sio:SIO_000628
miriam-gene:2072
,
lld:C0009207
;
a
sio:SIO_001121
.
}
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_provenance
{
dgn-np:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_assertion
dcterms:description
"[Cockayne syndrome (CS) cells and xeroderma pigmentosum (XP) cells (XPD, XPA, XPG, and XPF) were defective in Pol II degradation, whereas XPC cells whose defect is limited to global genome NER in nontranscribing regions were proficient for Pol II degradation.]. 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:18927284
;
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:NP403645.RAZI_SC4ka95OiRk_QH5gbo7p2szrqpxFp_90DYp0WVYU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}