@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80
> .
@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:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_head
{
this:
np:hasAssertion
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_assertion
;
np:hasProvenance
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_provenance
;
np:hasPublicationInfo
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_assertion
a
np:Assertion
.
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_provenance
a
np:Provenance
.
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_assertion
{
miriam-gene:796
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN86962e0b1eaac09a8a6621be3acfa0d8
sio:SIO_000628
miriam-gene:796
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_provenance
{
dgn-np:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_assertion
dcterms:description
"[Even if the gene is normally methylated in most cases of chronic myeloid leukemia (CML), we have found that the hypermethylation of the calcitonin gene marks progression of CML and precedes any other signs of acceleration with several months.]. 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:8322016
;
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:NP382410.RAoElirQPzsczyExDAzyc_ET47r10PSx6rKY2OIFpFt80130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}