@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g
> .
@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:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_head
{
this:
np:hasAssertion
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_assertion
;
np:hasProvenance
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_provenance
;
np:hasPublicationInfo
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_assertion
a
np:Assertion
.
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_provenance
a
np:Provenance
.
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_assertion
{
miriam-gene:9048
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNb37a017550e2d065940536ca6b93b1e8
sio:SIO_000628
miriam-gene:9048
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_provenance
{
dgn-np:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_assertion
dcterms:description
"[Our results suggest that this treatment modality of intrathecal transplantation of human NSCs genetically modified to overexpress neurotrophic factor(s) might be of value in the treatment of ALS patients without significant adverse 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:19626053
;
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:NP436879.RA0wX5oC0Uqarcp4WXiWujJmYhqm5oGaCkyoXYsZbt83g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}