@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M
> .
@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:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_head
{
this:
np:hasAssertion
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_assertion
;
np:hasProvenance
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_provenance
;
np:hasPublicationInfo
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_assertion
a
np:Assertion
.
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_provenance
a
np:Provenance
.
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_assertion
{
miriam-gene:6638
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNd2d76a5d86dead36a31160f782ec0a7b
sio:SIO_000628
miriam-gene:6638
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_provenance
{
dgn-np:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_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-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:NP316365.RACkscZyfF897J4v_nve6SMkYuRfCTabSjs4N3GMA-51M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}