@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA
> .
@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:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_head
{
this:
np:hasAssertion
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_assertion
;
np:hasProvenance
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_provenance
;
np:hasPublicationInfo
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_assertion
a
np:Assertion
.
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_provenance
a
np:Provenance
.
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_assertion
{
miriam-gene:4352
a
ncit:C16612
.
lld:C1527405
a
ncit:C7057
.
dgn-gda:DGN7d8c533b1a20f33058ebd2fe21d51645
sio:SIO_000628
miriam-gene:4352
,
lld:C1527405
;
a
sio:SIO_001121
.
}
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_provenance
{
dgn-np:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_assertion
dcterms:description
"[The recently discovered mutations in patients with CMD (V617F and exon 12 of JAK2 gene, MPL gene), and those identified in hereditary erythrocytosis and in hereditary thrombocytosis have improved our ability to discriminate these conditions.]. 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:18484677
;
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:NP375476.RASrhjpCe9plWQtB4wrnr_MJ-0CgGZBsCAYrQkgdKDApA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}