@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0
> .
@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:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_head
{
this:
np:hasAssertion
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_assertion
;
np:hasProvenance
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_provenance
;
np:hasPublicationInfo
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_assertion
a
np:Assertion
.
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_provenance
a
np:Provenance
.
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN8a213248d96ecea05521bf4181cd0aed
sio:SIO_000628
miriam-gene:3126
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_provenance
{
dgn-np:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_assertion
dcterms:description
"[We did not confirm that non-human leukocyte antigen polymorphisms were associated with outcomes in myeloablative unrelated donor hematopoietic cell transplantation for chronic myeloid leukemia, possibly because of the strong association between clinical variables and outcome which masked more subtle genetic effects.]. 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:22271889
;
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:NP299195.RAQMI3dqeL9Ppd5aVx-R5_OtCoKF-S5IIsZIPkX5oxej0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}