@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE
> .
@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:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_head
{
this:
np:hasAssertion
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_assertion
;
np:hasProvenance
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_provenance
;
np:hasPublicationInfo
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_assertion
a
np:Assertion
.
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_provenance
a
np:Provenance
.
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN9af41c50fe975e9927703a13aa3ef744
sio:SIO_000628
miriam-gene:2272
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_provenance
{
dgn-np:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_assertion
dcterms:description
"[We conclude that the abnormalities of FHIT, presumably associated with the unstable nature of FRA3B within the FHIT gene, are involved in the carcinogenesis of gastric cancer, and lack of mismatch repair (MMR) could possibly promote its alteration in a subset of gastric tumours.]. 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:11916557
;
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:NP185412.RAvxTciuoeJsLAb3mF8tFMlW5C8lZIn04KVviIaADZ-wE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}