@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4
> .
@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:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_head
{
this:
np:hasAssertion
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_assertion
;
np:hasProvenance
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_provenance
;
np:hasPublicationInfo
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_assertion
a
np:Assertion
.
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_provenance
a
np:Provenance
.
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_assertion
{
miriam-gene:2523
a
ncit:C16612
.
lld:C0027022
a
ncit:C7057
.
dgn-gda:DGN228287feacfcbe23db6def8ca3bce092
sio:SIO_000628
miriam-gene:2523
,
lld:C0027022
;
a
sio:SIO_001121
.
}
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_provenance
{
dgn-np:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_assertion
dcterms:description
"[Several hypotheses are under investigation such as differences in the targeted hematopoietic stem cells (HSC), host modifier polymorphisms, intensity of JAK2V617F signaling, presence of other somatic mutations, or the presence of a pre-JAK2 event that may vary according to the MPD phenotype.]. 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:19074061
;
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:NP879662.RAZSgMvjzTbdCOC8YSm07SSLJl5ManmqoNdXFVlJ8ySR4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}