@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0
> .
@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:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_head
{
this:
np:hasAssertion
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_assertion
;
np:hasProvenance
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_provenance
;
np:hasPublicationInfo
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_assertion
a
np:Assertion
.
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_provenance
a
np:Provenance
.
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_assertion
{
miriam-gene:1913
a
ncit:C16612
.
lld:C0040028
a
ncit:C7057
.
dgn-gda:DGN178551f54c5c502a5a51959af3cce979
sio:SIO_000628
miriam-gene:1913
,
lld:C0040028
;
a
sio:SIO_001121
.
}
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_provenance
{
dgn-np:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_assertion
dcterms:description
"[Increased PRV-1 expression was found in 37 out of 46 patients diagnosed with PV (80%), in 4 out of 15 patients diagnosed with essential thrombocythemia (ET) (27%) and in 4 out of 8 patients with chronic idiopathic myelofibrosis (CIMF) (50%), and increased PRV-1 expression plus EEC formation was observed in 19 of 36 examined MPD patients indicating the superiority of PVSG and WHO bone marrow criteria for the diagnosis of ET, PV and CIMF.]. 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:17852451
;
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:NP805243.RAe8SMZcrmlj_x0ecCtPmeU3ZxitFonVozb9LzUBDdHa0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}