@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_head
{
this:
np:hasAssertion
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_assertion
;
np:hasProvenance
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_assertion
a
np:Assertion
.
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_provenance
a
np:Provenance
.
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_assertion
{
miriam-gene:2067
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGNdab719981b494cf6eaa8382ee961b745
sio:SIO_000628
miriam-gene:2067
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_provenance
{
dgn-np:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_assertion
dcterms:description
"[NSCLC specimens that harboring EGFR-activating mutations are more likely to express low ERCC1 and high TUBB3 mRNA levels, whereas tumors from patients with NSCLC harboring KRAS mutation are more likely to express high ERCC1 mRNA levels.]. 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:24994038
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP381292.RA9B4tkwxS_8bg8UFQetpcmjT7hs7vi6F4Q72ciYdRRPQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:20+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}