@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU
> .
@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:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_head
{
this:
np:hasAssertion
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_assertion
;
np:hasProvenance
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_provenance
;
np:hasPublicationInfo
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_assertion
a
np:Assertion
.
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_provenance
a
np:Provenance
.
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_assertion
{
miriam-gene:7376
a
ncit:C16612
.
lld:C0033300
a
ncit:C7057
.
dgn-gda:DGN7a9c74cf274575127d3c7033208fdcd2
sio:SIO_000628
miriam-gene:7376
,
lld:C0033300
;
a
sio:SIO_001121
.
}
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_provenance
{
dgn-np:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_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-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:NP672161.RA7zOkazZLdSB9hQgn28aPbJQN7FjXGzMO3U1y90qiTXU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}