@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA
> .
@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:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_head
{
this:
np:hasAssertion
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_assertion
;
np:hasProvenance
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_provenance
;
np:hasPublicationInfo
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_assertion
a
np:Assertion
.
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_provenance
a
np:Provenance
.
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_assertion
{
miriam-gene:23221
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN871f4b09999305a2b6f61d24edee4a48
sio:SIO_000628
miriam-gene:23221
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_provenance
{
dgn-np:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_assertion
dcterms:description
"[One of the regions of loss of heterozygosity (LOH) on 8p22 identified in bladder cancer contains two genes, LZTS1 (FEZ1) and DBC2 (RHOBTB2) that have been shown to be mutated at low frequency in other 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:15922864
;
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:NP596624.RAa-wU_JyNvewIPpqnLuV0FjSZG7mPfVgHm5DWl2ii1TA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:58+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" .
}