@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU
> .
@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:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_head
{
this:
np:hasAssertion
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_assertion
;
np:hasProvenance
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_provenance
;
np:hasPublicationInfo
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_assertion
a
np:Assertion
.
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_provenance
a
np:Provenance
.
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_assertion
{
miriam-gene:3123
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNc8be2941570fa960c631b806b5984aa7
sio:SIO_000628
miriam-gene:3123
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_provenance
{
dgn-np:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_assertion
dcterms:description
"[This study examined the theoretical availability of compatible unrelated umbilical cord blood (UCB) units for hematopoietic stem cell transplantation (HSCT) of children with sickle cell disease (SCD), matched for DRB1 at high resolution.]. 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:16394889
;
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:NP408369.RABlz96V5-dEAlYNI3iilY5K4KdCemuj5hN_VLyuqcuXU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:03+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" .
}