@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc
> .
@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:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_head
{
this:
np:hasAssertion
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_assertion
;
np:hasProvenance
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_provenance
;
np:hasPublicationInfo
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_assertion
a
np:Assertion
.
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_provenance
a
np:Provenance
.
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0024121
a
ncit:C7057
.
dgn-gda:DGN2fbec757d27f2d63f9783f4b23f803fd
sio:SIO_000628
miriam-gene:189
,
lld:C0024121
;
a
sio:SIO_001121
.
}
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_provenance
{
dgn-np:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_assertion
dcterms:description
"[Heterogeneity in the level of AGT expressed in different lung cell populations or other forms of carcinogenic DNA damage caused by NNK may explain the residual incidence of lung tumors in MGMT transgenic mice.]. 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:10069465
;
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:NP476210.RAaarFpN-cMgrDq7XQfoN3u9nfjd8ewsmVNx8QaVidvhc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}