@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI
> .
@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:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_head
{
this:
np:hasAssertion
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_assertion
;
np:hasProvenance
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_assertion
a
np:Assertion
.
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_provenance
a
np:Provenance
.
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_assertion
{
miriam-gene:3214
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGN1f0322b1e072a3f00a9256bd6d72fff6
sio:SIO_000628
miriam-gene:3214
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_provenance
{
dgn-np:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_assertion
dcterms:description
"[To evaluate the contribution of bone marrow (BM) cells to treat neurological disorders, we examined the effectiveness of BM cells expressing the homeobox B4 (HoxB4) gene to cure mice with metachromatic leukodystrophy (MLD) through transplantation.]. 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:20424597
;
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:NP253037.RAjmT31-LPxlZX9ezO-dYc5UHXe8SkhoJ_WdipUpXnPUI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}