@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k
> .
@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:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_head
{
this:
np:hasAssertion
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion
;
np:hasProvenance
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion
a
np:Assertion
.
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_provenance
a
np:Provenance
.
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGN8d2c73920d6230d90c8e95eb274b1cf2
sio:SIO_000628
miriam-gene:3717
,
lld:C0027022
;
a
sio:SIO_001122
.
}
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_provenance
{
dgn-np:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_assertion
dcterms:description
"[ARMS-PCR technique can be used to detect the frequency and mutational status of JAK2V617F mutation owing to its sensitivity and along with capillary electrophoresis, quantitative assay for mutated JAK2 mRNA, diagnosis of CMPD and judgement of prognosis become possible.]. 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:19549471
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP71500.RA9zsmkZ7uq3hB9DYFYM_c5tiE56II2FItD7gb_hZKc9k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}