@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys
> .
@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:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_head
{
this:
np:hasAssertion
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion
;
np:hasProvenance
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_provenance
;
np:hasPublicationInfo
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion
a
np:Assertion
.
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_provenance
a
np:Provenance
.
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion
{
miriam-gene:10721
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN75d231bb0d9989fd0a82bc1e91ff25eb
sio:SIO_000628
miriam-gene:10721
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_provenance
{
dgn-np:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_assertion
dcterms:description
"[XP cells were found to have defects in seven of the proteins of the nucleotide excision repair pathway and in DNA polymerase η. XP cells are hypersensitive to killing by UV radiation, and XP cancers have characteristic `UV signature` mutations.]. 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:22217736
;
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:NP194150.RAXCaSoGAj4kwdQ6MQYxyqoDDTYZV12diT_Xf4sUpn_ys130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}