@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo
> .
@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:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_head
{
this:
np:hasAssertion
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_assertion
;
np:hasProvenance
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_provenance
;
np:hasPublicationInfo
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_assertion
a
np:Assertion
.
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_provenance
a
np:Provenance
.
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN7ee5ed94427f0855028a0c655a84f4bc
sio:SIO_000628
miriam-gene:2272
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_provenance
{
dgn-np:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_assertion
dcterms:description
"[To correlate DNA and RNA lesions of the FHIT gene with the effect on FHIT protein expression, we have investigated the FHIT gene for loss of heterozygosity (LOH), aberrant transcripts, point mutations, and protein expression in 35 gastric adenocarcinomas.]. 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:11396980
;
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:NP541677.RA7tkRPQeEwRTRXIv8HkiOX-GOo-lyfCKUxZBK6rMNmWo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}