@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro
> .
@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:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_head
{
this:
np:hasAssertion
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_assertion
;
np:hasProvenance
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_provenance
;
np:hasPublicationInfo
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_assertion
a
np:Assertion
.
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_provenance
a
np:Provenance
.
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGNf53290094395feda2d324722e9407c43
sio:SIO_000628
miriam-gene:1728
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_provenance
{
dgn-np:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_assertion
dcterms:description
"[Furthermore, cell lines genotyped homozygous for the 609T allele showed significantly lower NQO1 protein expression and higher sensitivity for amrubicinol than those with the other genotypes in both NSCLC and SCLC cells.]. 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:21964527
;
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:NP351192.RARqXamUqdRI54Nw4yDUAtNYgL___B7_Jy788OXaOvHro130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}