@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM
> .
@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:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_head
{
this:
np:hasAssertion
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_assertion
;
np:hasProvenance
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_assertion
a
np:Assertion
.
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_provenance
a
np:Provenance
.
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_assertion
{
miriam-gene:5293
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN53081d31018f95c1ebb803a435043d10
sio:SIO_000628
miriam-gene:5293
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_provenance
{
dgn-np:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_assertion
dcterms:description
"[Aberrant activation of PI3K/AKT signalling represents one of the most common molecular alterations in lung cancer, though the relative contribution of the single components of the cascade to the NSCLC development is still poorly defined.]. 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:22363436
;
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:NP220556.RAh_hw0bH2Xc2KC0M1fSxTvruHamN8g4O--Pjm4xORGjM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}