@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w
> .
@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/
> .
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_head
{
this:
np:hasAssertion
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_assertion
;
np:hasProvenance
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_provenance
;
np:hasPublicationInfo
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_assertion
a
np:Assertion
.
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_provenance
a
np:Provenance
.
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGNd028a81e80145926589e7305ae909269
sio:SIO_000628
miriam-gene:3717
,
lld:C0027022
;
a
sio:SIO_001122
.
}
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_provenance
{
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_assertion
dcterms:description
"[Determination of the JAK2 V617F mutation may contribute to the search for genetic determinants of PMVT and may be useful to recognize patients who should be carefully observed for the subsequent development of overt MPDs.]. 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:17059429
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
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 .
}
dgn-np:NP575733.RAwVAzK-oCrLGrKhaabLPE1LUulDHV42eu0KP1qLGCu3w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:06+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}