@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU
> .
@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:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_head
{
this:
np:hasAssertion
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_assertion
;
np:hasProvenance
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_assertion
a
np:Assertion
.
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_provenance
a
np:Provenance
.
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_assertion
{
miriam-gene:2523
a
ncit:C16612
.
lld:C0162309
a
ncit:C7057
.
dgn-gda:DGN06fb40a18d335e1008bc89a5b8326d39
sio:SIO_000628
miriam-gene:2523
,
lld:C0162309
;
a
sio:SIO_001121
.
}
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_provenance
{
dgn-np:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_assertion
dcterms:description
"[Longer follow-up of these two treated patients and HSC gene therapy performed in additional ALD patients are however needed to evaluate the safety and efficacy of lentiviral HSC gene therapy in cerebral forms of X-ALD.]. 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:22365775
;
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:NP597691.RA1StnoWln3ETTTpg2dK1THXRjEeBRz6oP181tzPZDBCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}