@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw
> .
@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:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_head
{
this:
np:hasAssertion
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_assertion
;
np:hasProvenance
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_provenance
;
np:hasPublicationInfo
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_assertion
a
np:Assertion
.
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_provenance
a
np:Provenance
.
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGNa57dc5a304b89533d242efa7316ec10e
sio:SIO_000628
miriam-gene:5290
,
lld:C0546837
;
a
sio:SIO_001121
.
}
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_provenance
{
dgn-np:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_assertion
dcterms:description
"[No somatic changes were detected in PIK3CB This study extends previous observations in other tumor types by demonstrating the presence of somatic PIK3CA mutations in both SCC and adenocarcinoma of the esophagus, thus implicating the PI3K pathway in the initiation and/or progression of esophageal cancers.]. 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:16380997
;
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:NP691318.RAn96LQBeitXQO66il-kEOVlTod4s7T9YAnNnLOZMgdSw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}