@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg
> .
@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:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_head
{
this:
np:hasAssertion
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_assertion
;
np:hasProvenance
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_provenance
;
np:hasPublicationInfo
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_assertion
a
np:Assertion
.
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_provenance
a
np:Provenance
.
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_assertion
{
miriam-gene:1950
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN7c737a7c2982fa574de16ed2bc3b7f3d
sio:SIO_000628
miriam-gene:1950
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_provenance
{
dgn-np:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_assertion
dcterms:description
"[Compensatory activation of related ERBB family receptors (ERBB2 and ERBB3) was observed in GBM CSCs deprived of EGFR signal (EGF deprivation or cetuximab inhibition), suggesting an intrinsic GBM resistance mechanism for EGFR-targeted therapy.]. 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:22745588
;
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:NP163795.RAA9tlyKP9vVWHDDIlINR31WogVcBIlTg3M2g_UXUJ6pg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}