@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg
> .
@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:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_head
{
this:
np:hasAssertion
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_assertion
;
np:hasProvenance
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_provenance
;
np:hasPublicationInfo
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_assertion
a
np:Assertion
.
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_provenance
a
np:Provenance
.
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C1520166
a
ncit:C7057
.
dgn-gda:DGNe20f782f83e82915181e9d58db995cc9
sio:SIO_000628
miriam-gene:1956
,
lld:C1520166
;
a
sio:SIO_001121
.
}
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_provenance
{
dgn-np:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_assertion
dcterms:description
"[In this study, we investigated the effects of the combination of Erlotinib and Cetuximab on T790M and L858R mutation lung cancer cells lines (H1975), in the primary NSCLC cells with the T790M mutation and TKI-resistant EGFR mutations human tumor xenograft model (H1975).]. 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:22821179
;
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:NP511923.RAe9NPvAA_7SRTiOgGlULh9_5C-hiRbmtERMj8GJQnNlg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}