@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E
> .
@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:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_head
{
this:
np:hasAssertion
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_assertion
;
np:hasProvenance
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_provenance
;
np:hasPublicationInfo
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_assertion
a
np:Assertion
.
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_provenance
a
np:Provenance
.
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0432411
a
ncit:C7057
.
dgn-gda:DGNd07793816b96a83bba6bd5cb3f9b8a9f
sio:SIO_000628
miriam-gene:3717
,
lld:C0432411
;
a
sio:SIO_001121
.
}
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_provenance
{
dgn-np:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_assertion
dcterms:description
"[Consistent with the concept of distinct pathogenetic mechanisms, we show that patients with and without the JAK2 mutation have different patterns of cytogenetic abnormality, with virtually all patients carrying the 20q deletion or trisomy 9 being V617F(+).]. 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:16873677
;
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:NP331263.RAbchLIaryoPG0qCpj_MM2xnmgUptQRgtI8QTgOWRw9_E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}