@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q
> .
@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:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_head
{
this:
np:hasAssertion
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion
;
np:hasProvenance
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion
a
np:Assertion
.
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_provenance
a
np:Provenance
.
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion
{
miriam-gene:259197
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNfe8a5ece70331f9bd66048734b41fb09
sio:SIO_000628
miriam-gene:259197
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_provenance
{
dgn-np:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_assertion
dcterms:description
"[Our longitudinal study of AML patients showed that the NCR(dull) phenotype was acquired during leukemia development because we observed its complete (for NKp46) or partial (for NKp30) reversibility in patients achieving complete remission (CR).]. 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:16940427
;
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:NP395407.RACyNogsHdso0Cipq5QNWyE575DqD49m7PR_-FqH89M3Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}