@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM
> .
@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:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_head
{
this:
np:hasAssertion
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_assertion
;
np:hasProvenance
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_assertion
a
np:Assertion
.
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_provenance
a
np:Provenance
.
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGN7c1eb299a12c76d35ca341f91512751e
sio:SIO_000628
miriam-gene:1030
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_provenance
{
dgn-np:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_assertion
dcterms:description
"[To clarify the role of fragile histidine triad (FHIT) in hematological malignancies, we examined the methylation status and the expression level of the FHIT gene in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML) cells in comparison with the methylation of the p15(INK4B) gene.]. 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:15902282
;
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:NP903466.RAp7ixBtpEQW0m__006qnmsCEz888bnJ9dZ6iMnVifeMM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}