@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug
> .
@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:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_head
{
this:
np:hasAssertion
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion
;
np:hasProvenance
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_provenance
;
np:hasPublicationInfo
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion
a
np:Assertion
.
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_provenance
a
np:Provenance
.
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C0940937
a
ncit:C7057
.
dgn-gda:DGNacf0a3d92a21a1b28814542d90129db7
sio:SIO_000628
miriam-gene:2272
,
lld:C0940937
;
a
sio:SIO_001121
.
}
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_provenance
{
dgn-np:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_assertion
dcterms:description
"[More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of allele deletion in precancerous lesions and 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:20082323
;
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:NP782060.RAyBfDHnTa6iszvZKENuMC-O5DllzSxOU8CPJyGru6iug130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}