@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_assertion
a
np:Assertion
.
dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_provenance
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np:Provenance
.
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.
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dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGNd63f4a3984df269c80a9e16946514837
sio:SIO_000628
miriam-gene:3717
,
lld:C0001815
;
a
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.
}
dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_provenance
{
dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_assertion
dcterms:description
"[However, it is very clear that some patients with classical PV lack the JAK2 V617F mutation, while some patients with other chronic myeloproliferative disorders such as idiopathic myelofibrosis (IMF) and essential thrombocytosis (ET) also express the JAK2 V617F mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:16210034
;
prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP516817.RAGolvifkC5AguvD3nSZffjlOEUcgnBUCbXngqxAXDasU130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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
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"v4.0.0" .
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