@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q
> .
@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:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_head
{
this:
np:hasAssertion
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_assertion
;
np:hasProvenance
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_assertion
a
np:Assertion
.
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_provenance
a
np:Provenance
.
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0012860
a
ncit:C7057
.
dgn-gda:DGNb7d4670bde380bc3892480552b719850
sio:SIO_000628
miriam-gene:2068
,
lld:C0012860
;
a
sio:SIO_001122
.
}
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_provenance
{
dgn-np:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_assertion
dcterms:description
"[our data suggest that the genotypes of CYP2E1, XRCC1 194, and XPD 751 were associated with the level of DNA damage and may contribute to individual sensitivity to DNA damage induced by VCM in the workplace.]. 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:18420361
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP75382.RA8R9TK6rooGpcXICnvdMTCOPUcbh-Nh5AuKqTzzsu40Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}