@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg
> .
@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:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_head
{
this:
np:hasAssertion
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_assertion
;
np:hasProvenance
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_provenance
;
np:hasPublicationInfo
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_assertion
a
np:Assertion
.
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_provenance
a
np:Provenance
.
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0278701
a
ncit:C7057
.
dgn-gda:DGN7a921c6ca7d60d596c8aa0728a865580
sio:SIO_000628
miriam-gene:7248
,
lld:C0278701
;
a
sio:SIO_001121
.
}
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_provenance
{
dgn-np:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_assertion
dcterms:description
"[LOH mapping showed allelic losses were widespread on both chromosomes and suggests the possibility that multiple tumour suppressor genes, including one or more that are unknown, might be inactivated in the aetiology of gastric adenocarcinoma.]. 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:18380938
;
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:NP570547.RAkCgfS2B3-a5xsqxad3yUoSzz7Bg3oNJxsW2PamE0HFg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}