@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU
> .
@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:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_head
{
this:
np:hasAssertion
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_assertion
;
np:hasProvenance
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_provenance
;
np:hasPublicationInfo
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_assertion
a
np:Assertion
.
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_provenance
a
np:Provenance
.
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0546837
a
ncit:C7057
.
dgn-gda:DGN8e37ac116d9ade2039f53f007e6a5521
sio:SIO_000628
miriam-gene:2272
,
lld:C0546837
;
a
sio:SIO_001121
.
}
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_provenance
{
dgn-np:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_assertion
dcterms:description
"[These data suggest that the open reading frame of FHIT is not important in the development or progression of most primary esophageal carcinomas or UCANs, although lack of expression of the FHIT transcript may be common in esophageal cancer-derived cell lines.]. 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:9233782
;
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:NP357335.RAog8Im0OPGCnTXqDC4VAkuAnMfcBcTd-H2VihUmE8GjU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:29+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" .
}