@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY
> .
@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:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_head
{
this:
np:hasAssertion
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_assertion
;
np:hasProvenance
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_provenance
;
np:hasPublicationInfo
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_assertion
a
np:Assertion
.
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_provenance
a
np:Provenance
.
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_assertion
{
miriam-gene:5429
a
ncit:C16612
.
lld:C0263581
a
ncit:C7057
.
dgn-gda:DGNb2a8d10d125319b0b31a876c1105acc3
sio:SIO_000628
miriam-gene:5429
,
lld:C0263581
;
a
sio:SIO_001121
.
}
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_provenance
{
dgn-np:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_assertion
dcterms:description
"[The variant type of XP (XPV), first described in 1970 by Ernst G. Jung as 'pigmented xerodermoid', is caused by defects in the post replication repair machinery while NER is not impaired.]. 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:14705792
;
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:NP264548.RAyljtkQiQ4thP_qAr3QbBZ-MLHqaitfy2faeq8E2u3TY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}