@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE
> .
@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 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:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_head
{
this:
np:hasAssertion
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_assertion
;
np:hasProvenance
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_assertion
a
np:Assertion
.
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_provenance
a
np:Provenance
.
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_assertion
{
miriam-gene:9734
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN2351a7db1e9dbce4d5a2c1866180ee32
sio:SIO_000628
miriam-gene:9734
,
lld:C0007131
;
a
sio:SIO_001122
.
}
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_provenance
{
dgn-np:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_assertion
dct:description
"[All together, our results show that genome wide patterns of alteration differ between EGFR and KRAS mutated lung ADC, describe two models of oncogenic cooperation involving either EGFR mutation and CDKN2A deletion or cyclin amplification and TP53 inactiva]. 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:18549475
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP79374.RAxisBzIr6rBr3EBiSUgbFClXcCqc2YqIZcA-dNPFOFBE130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}