@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U
> .
@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:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_head
{
this:
np:hasAssertion
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion
;
np:hasProvenance
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_provenance
;
np:hasPublicationInfo
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion
a
np:Assertion
.
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_provenance
a
np:Provenance
.
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion
{
miriam-gene:3417
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN4d63b891ba9182f623e627ae66974a36
sio:SIO_000628
miriam-gene:3417
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_provenance
{
dgn-np:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_assertion
dcterms:description
"[We investigated the IDH1 gene mutation status by nested PCR and denaturing gradient gel electrophoresis (DGGE) on DNA extracted from archival tumor blocks of 63 glioma patients who were treated following recurrence with the epidermal growth factor receptor (EGFR)-targeted blocking monoclonal antibody cetuximab, or the vascular endothelial growth factor (receptor) (VEGF(R))-targeted agents sunitinib malate and bevacizumab.]. 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:22199315
;
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:NP766073.RAEF_fKN_NgsF9uT1xj655u7vFr6lcseUA9FCxiOH0x-U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}