@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw
> .
@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:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_head
{
this:
np:hasAssertion
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_assertion
;
np:hasProvenance
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_provenance
;
np:hasPublicationInfo
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_assertion
a
np:Assertion
.
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_provenance
a
np:Provenance
.
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNfa08279dea613d433cca5c726dea4c95
sio:SIO_000628
miriam-gene:2272
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_provenance
{
dgn-np:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_assertion
dcterms:description
"[These results suggested that aberrant methylation of the FHIT gene might be one of molecular events involved in the disease progression of MDS and be an adverse prognostic factor in MDS.]. 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:18367246
;
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:NP408796.RAYxx9IghQNVS1WFTbElno_5srkdEOilKTaAlFSFcyibw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}