@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk
> .
@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:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_head
{
this:
np:hasAssertion
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion
;
np:hasProvenance
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_provenance
;
np:hasPublicationInfo
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion
a
np:Assertion
.
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_provenance
a
np:Provenance
.
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion
{
miriam-gene:3717
a
ncit:C16612
.
lld:C1292778
a
ncit:C7057
.
dgn-gda:DGN107f5bb494b4daa6366b3b84f9c09501
sio:SIO_000628
miriam-gene:3717
,
lld:C1292778
;
a
sio:SIO_001121
.
}
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_provenance
{
dgn-np:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_assertion
dcterms:description
"[A point mutation in the Janus tyrosine kinase 2 (JAK2) gene has been described in patients with chronic myeloproliferative disorders (MPD), but the clinical significance of JAK2(V617F), which may be harbored in either the heterozygote or homozyote status, is still largely undefined.]. 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:16572198
;
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:NP165156.RArse7e9SFBkbjpSrcj8w_DtSO7WkiG80uzH78kQzN9sk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}