@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM
> .
@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:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_head
{
this:
np:hasAssertion
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_assertion
;
np:hasProvenance
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_provenance
;
np:hasPublicationInfo
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_assertion
a
np:Assertion
.
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_provenance
a
np:Provenance
.
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNaf85f25107f2bf2609477d78958c5c70
sio:SIO_000628
miriam-gene:2272
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_provenance
{
dgn-np:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_assertion
dcterms:description
"[Because the fragile histidine triad (FHIT) gene, a tumor suppressor gene encompassing the most active, common fragile site FRA3B, is frequently deleted in various cancers, we evaluated the expression of WWOX and FHIT in 74 cases of primary hematopoietic neoplasias and 20 leukemia 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:14638866
;
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:NP576303.RA98nsUAlFs03Nhu4rI6Etx_m5nn613fKQBskAhANrxgM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}