@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_head
{
this:
np:hasAssertion
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_assertion
;
np:hasProvenance
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_provenance
;
np:hasPublicationInfo
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_assertion
a
np:Assertion
.
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_provenance
a
np:Provenance
.
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_assertion
{
miriam-gene:3925
a
ncit:C16612
.
lld:C0085084
a
ncit:C7057
.
dgn-gda:DGN9f2663f41d013b760996d8b6dbc40e97
sio:SIO_000628
miriam-gene:3925
,
lld:C0085084
;
a
sio:SIO_001121
.
}
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_provenance
{
dgn-np:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_assertion
dcterms:description
"[The association between survivor motor neuron (SMN) gene deletions and motor neuron diseases such as spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS) suggest that sporadic lower motor neuron disease (LMND) may be related to SMN gene deletion.]. 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:20947812
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP845768.RAPvRXHaSvLE6lwg19VzG1TbILQ8knghdgN7BnwS0UMXs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}