@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg
> .
@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:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_head
{
this:
np:hasAssertion
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_assertion
;
np:hasProvenance
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_provenance
;
np:hasPublicationInfo
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_assertion
a
np:Assertion
.
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_provenance
a
np:Provenance
.
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_assertion
{
miriam-gene:4352
a
ncit:C16612
.
lld:C0001815
a
ncit:C7057
.
dgn-gda:DGNdb99cad6a719ff15c859541be04ccf22
sio:SIO_000628
miriam-gene:4352
,
lld:C0001815
;
a
sio:SIO_001121
.
}
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_provenance
{
dgn-np:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_assertion
dcterms:description
"[For instance, the presence of a JAK2 mutation is now considered conditio sine qua non for the diagnosis of PV and the World Health Organization classification system has recently revised its diagnostic criteria for PV, ET, and PMF to include JAK2 and MPL mutations as clonal markers.]. 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:18429051
;
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:NP667229.RATlX7THdSBKNfr0lXCvKhLAbphYoM-3LDipxxv6Conlg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:47+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: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" .
}