@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA
> .
@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:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_head
{
this:
np:hasAssertion
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_assertion
;
np:hasProvenance
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_assertion
a
np:Assertion
.
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_provenance
a
np:Provenance
.
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_assertion
{
miriam-gene:4597
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNd155b25bbca9fef619b5318c10f3fdce
sio:SIO_000628
miriam-gene:4597
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_provenance
{
dgn-np:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_assertion
dcterms:description
"[We conclude that del(5q), although most prevalent in MDS, is seen across the spectrum of myeloid disorders including MPD and its occurrence in lymphoid disorders might signify, for the most part, an occult myeloid clone.]. 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:17707907
;
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:NP238993.RA5AuoZIiHkZmb-LGMo_X7an8UA27XHfO6lDrvfrTCrUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}