@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_assertion
;
np:hasProvenance
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dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_assertion
a
np:Assertion
.
dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_provenance
a
np:Provenance
.
dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN12f7fc3be90372e978bb02d7b2bfc782
sio:SIO_000628
miriam-gene:2068
,
lld:C0008626
;
a
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.
}
dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_provenance
{
dgn-np:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_assertion
dcterms:description
"[Our study is focused on the extent of any such chromosomal aberrations with respect to chromium levels in the blood of welders as well as on the tentative modulating role of polymorphisms in DNA repair genes XPD Lys751Gln, XPG Asn114His, XPC Lys939Gln, hOGG1 Ser326Cys and XRCC1 Arg399Gln on chromosomal damage.]. 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:21858514
;
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:NP368704.RAtJHuf8zQi5ToUAF2NozZmhNCJPt6sTLKgcyLrHCIF_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:35+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
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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