@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_assertion
a
np:Assertion
.
dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_provenance
a
np:Provenance
.
dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_assertion
{
miriam-gene:3440
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN53887f4383912bde9b198c3de8b46ce9
sio:SIO_000628
miriam-gene:3440
,
lld:C0023473
;
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.
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dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_provenance
{
dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_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-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 .
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dgn-np:NP445254.RAuHGOrraDJB2YWsx3GBRi1mSN5v-IqHZpk9ACmH4Ty64130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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
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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
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