@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg
> .
@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:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_head
{
this:
np:hasAssertion
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_assertion
;
np:hasProvenance
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_provenance
;
np:hasPublicationInfo
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_assertion
a
np:Assertion
.
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_provenance
a
np:Provenance
.
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_assertion
{
miriam-gene:65125
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN0d98cf06cf5ad4bb9b3efeb0bdc9b3dd
sio:SIO_000628
miriam-gene:65125
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_provenance
{
dgn-np:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_assertion
dcterms:description
"[To infer relevant and specific pathway activation downstream of EGFR from gene expression in HNSCC, we generated gene expression signatures using immortalized keratinocytes (HaCaT) subjected to ligand stimulation and transfected with EGFR, RELA/p65, or HRASVal12D.]. 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:22549044
;
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:NP637599.RAPHsEUVyh-l4S4E-JGphwA8t8ASNht3XaIMPnHMUv7yg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}