@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24
> .
@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:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_head
{
this:
np:hasAssertion
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion
;
np:hasProvenance
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_provenance
;
np:hasPublicationInfo
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion
a
np:Assertion
.
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_provenance
a
np:Provenance
.
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion
{
miriam-gene:83886
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN0616aa59124f647aabc408a5a39cdab3
sio:SIO_000628
miriam-gene:83886
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_provenance
{
dgn-np:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_assertion
dcterms:description
"[Genetic analysis of MPN patient cohorts with adequate sample size and clear clinical annotation are needed to understand the importance of these mutations on MPN phenotype, risk of transformation to leukemia, response to therapy, and influence on overall survival.]. 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:23009937
;
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:NP211796.RAcwpw6_nMRBCQNss92KoEhZLRsgGjgjCj_wYJrvuQI24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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" .
}