@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_assertion
a
np:Assertion
.
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_provenance
a
np:Provenance
.
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:6607
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN0dfea9a421e0337fb1b36da7cc98bbc0
sio:SIO_000628
miriam-gene:6607
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_provenance
{
dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_assertion
dcterms:description
"[This review attempts to highlight some of the recent advances made in the understanding of the disease and how loss of the ubiquitously expressed survival of motor neurons (SMN) protein results in the SMA phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:16364894
;
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 .
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dgn-np:NP527674.RA1osE0U1yam9JAAwsgqeg1ktBxY9IYhLvWcObB61EkTA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:44+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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
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"v4.0.0" .
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