@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg
> .
@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:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_head
{
this:
np:hasAssertion
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_assertion
;
np:hasProvenance
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_provenance
;
np:hasPublicationInfo
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_assertion
a
np:Assertion
.
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_provenance
a
np:Provenance
.
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN1cb051c2018c792eea1da88931093b1d
sio:SIO_000628
miriam-gene:207
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_provenance
{
dgn-np:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_assertion
dcterms:description
"[Epidermal growth factor receptor (EGFR) gene amplification is one of the most common genetic changes in glioblastoma and can lead to the activation of various downstream signaling molecules, including STAT3, MAPK, and AKT.]. 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:17146292
;
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:NP393578.RAekseRxp55-gq0RP0YHDZpxljXCOGaWOieDjXVeJ1Xsg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}