@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU
> .
@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:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_head
{
this:
np:hasAssertion
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_assertion
;
np:hasProvenance
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_provenance
;
np:hasPublicationInfo
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_assertion
a
np:Assertion
.
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_provenance
a
np:Provenance
.
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_assertion
{
miriam-gene:2669
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGNd539c6c5a4dc79a40cdce450172594bb
sio:SIO_000628
miriam-gene:2669
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_provenance
{
dgn-np:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_assertion
dcterms:description
"[In 178 patients receiving T-cell-depleted HLA-identical sibling transplants for acute myelogenous leukemia (AML), chronic myelogenous leukemia (CML), acute lymphoblastic leukemia (ALL), or myelodysplastic syndrome (MDS), analysis of donor KIR genotype with HLA genotype demonstrated that 62.9% of the patients lacked an HLA ligand for donor-inhibitory KIR.]. 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:15731175
;
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:NP277038.RACj8UTlu7zpZSmf-Tj6ZMtjteSxZO682CFNxPmIcIgdU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}