@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58
> .
@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:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_head
{
this:
np:hasAssertion
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion
;
np:hasProvenance
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_provenance
;
np:hasPublicationInfo
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion
a
np:Assertion
.
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_provenance
a
np:Provenance
.
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion
{
miriam-gene:4082
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGNebab7a5f5b367100fdc90ea6cd671b96
sio:SIO_000628
miriam-gene:4082
,
lld:C0001815
;
a
sio:SIO_001121
.
}
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_provenance
{
dgn-np:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_assertion
dcterms:description
"[A combination of magnetic cell sorting (MACS) and fluorescent in situ hybridization (FISH) techniques was used to detect clonal cytogenetic markers in different myeloid and lymphoid cell types of the peripheral blood from 4 patients with myelofibrosis with myeloid metaplasia (MMM) that was associated with either a 13q- or a 20q- karyotypic abnormality.]. 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:12406879
;
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:NP673332.RArvXwyFpRvOk4Z8GycH1BbuyujKacWVZYIlYiQsGlB58130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}