@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA
> .
@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:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_head
{
this:
np:hasAssertion
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_assertion
;
np:hasProvenance
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_provenance
;
np:hasPublicationInfo
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_assertion
a
np:Assertion
.
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_provenance
a
np:Provenance
.
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN2f214ce61c0893999e85c94036feb6e0
sio:SIO_000628
miriam-gene:3342
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_provenance
{
dgn-np:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_assertion
dcterms:description
"[To characterize phenotypic and genotypic changes in gastric cancer (GC), DNA copy number aberrations (CNAs) were assessed in 53 tumors using comparative genomic hybridization (CGH) and correlated with clinicopathologic characteristics and status of TP53 and replication error (RER).]. 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:11107179
;
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:NP280398.RAKBbVGsERDbqFokIP1K567pXmdDwSvcob0GQY1_76AvA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}