@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_head
{
this:
np:hasAssertion
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_assertion
;
np:hasProvenance
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_assertion
a
np:Assertion
.
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_provenance
a
np:Provenance
.
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0033300
a
ncit:C7057
.
dgn-gda:DGNfecc590693bc35d8b5c111f3765d1be6
sio:SIO_000628
miriam-gene:2068
,
lld:C0033300
;
a
sio:SIO_001121
.
}
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_provenance
{
dgn-np:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_assertion
dcterms:description
"[More strikingly, genetic defects in the same NER pathway, and in some cases even within the same gene, XPD, can also give rise to disorders with greatly elevated cancer rates but without progeria (xeroderma pigmentosum).]. 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:17172862
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP584598.RAvYgtBA8zjigZT11kfwptThj5Q7SRi3EqWK3ONy5kMA8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:10+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}