@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk
> .
@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:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_head
{
this:
np:hasAssertion
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion
;
np:hasProvenance
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_provenance
;
np:hasPublicationInfo
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion
a
np:Assertion
.
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_provenance
a
np:Provenance
.
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0238461
a
ncit:C7057
.
dgn-gda:DGN75270005046e993d4bffac0c3dc9872b
sio:SIO_000628
miriam-gene:1956
,
lld:C0238461
;
a
sio:SIO_001121
.
}
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_provenance
{
dgn-np:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_assertion
dcterms:description
"[Despite the low incidence of somatic EGFR gene mutation and amplification in the study samples, in view of the fact that high polysomy was often identified by FISH, as well as the current lack of therapeutic options, EGFR TKIs are worth investigating for treating the patients with ATC who have at least giant cell subtype.]. 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:17079354
;
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:NP440486.RAWJbRJKEpkElHdzdIGAubzoyhSbzXDOhOGPh43rW_5Rk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}