@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_assertion
;
np:hasProvenance
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_provenance
;
np:hasPublicationInfo
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_assertion
a
np:Assertion
.
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_provenance
a
np:Provenance
.
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_assertion
{
miriam-gene:4352
a
ncit:C16612
.
lld:C0032461
a
ncit:C7057
.
dgn-gda:DGNc16577f7414feb6042f38e68eb098a47
sio:SIO_000628
miriam-gene:4352
,
lld:C0032461
;
a
sio:SIO_001121
.
}
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_provenance
{
dgn-np:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_assertion
dcterms:description
"[Given their diagnostic relevance, it is also beneficial and relatively straightforward to screen JAK2 V617F negative patients for JAK2 exon 12 mutations (in the case of erythrocytosis) or MPL exon 10 mutations (thrombocytosis or myelofibrosis) using appropriate assays.]. 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:23057517
;
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:NP194181.RAHDPjHfF-sVWfuB1QIfpIqKUh-atbb2MJ9WsTCqEa5aw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}