@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y
> .
@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:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_head
{
this:
np:hasAssertion
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_assertion
;
np:hasProvenance
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_assertion
a
np:Assertion
.
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_provenance
a
np:Provenance
.
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_assertion
{
miriam-gene:8909
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGN5ec5eeb0eb9d62ea60438564f86094dd
sio:SIO_000628
miriam-gene:8909
,
lld:C0001815
;
a
sio:SIO_001121
.
}
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_provenance
{
dgn-np:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_assertion
dcterms:description
"[We report an elderly patient who presented with primary myelofibrosis (MF) with myeloid metaplasia (MMM), associated with idic(17)(p11.2) as the sole chromosomal abnormality, making this the first idic(17)(p11.2) myeloproliferative case reported in which the breakpoints are mapped to the breakpoint cluster region in proximal 17p.]. 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:16044457
;
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:NP778638.RAPfD0K6sBf7ExPZ5UzKST5WrhF4HxkrjRQKPMoE2Kx5Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}