@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo
> .
@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:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_head
{
this:
np:hasAssertion
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_assertion
;
np:hasProvenance
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_provenance
;
np:hasPublicationInfo
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_assertion
a
np:Assertion
.
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_provenance
a
np:Provenance
.
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNdc123f73a6fd79eb3908de1dbc7fd0e6
sio:SIO_000628
miriam-gene:7515
,
lld:C1956346
;
a
sio:SIO_001122
.
}
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_provenance
{
dgn-np:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_assertion
dcterms:description
"[We also investigated the presence of DNA damage in the peripheral lymphocytes of patients with CAD by using the micronucleus (MN) test and the effect of XPD Lys751Gln and XRCC1 Arg399Gln polymorphisms on this 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:18043991
;
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:NP92799.RAEWB3n6u61bdszCnKVE-d8ldp5sCqcPZBP_tFzNSAJUo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:46+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" .
}