@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_assertion
a
np:Assertion
.
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_provenance
a
np:Provenance
.
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3456
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN402bc5ae754d1736181f9b0637992f9b
sio:SIO_000628
miriam-gene:3456
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_provenance
{
dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_assertion
dcterms:description
"[In this paper we have performed the molecular studies of IFNA and IFNB genes in chronic myeloid leukemia (CML) in order to determine if the deletions of these genes are prevalent in this pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:7544849
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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 .
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dgn-np:NP478654.RAollsl888fHo6EmHq9OuF5A_0-ctiP59t_m7qmaes0aM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:22+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v3.0.0.0" .
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"v3.0.0" .
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