@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0
> .
@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:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_head
{
this:
np:hasAssertion
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_assertion
;
np:hasProvenance
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_provenance
;
np:hasPublicationInfo
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_assertion
a
np:Assertion
.
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_provenance
a
np:Provenance
.
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_assertion
{
miriam-gene:6638
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN546acd9118b6a2b190c51613c011a4ac
sio:SIO_000628
miriam-gene:6638
,
lld:C0026847
;
a
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.
}
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_provenance
{
dgn-np:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_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
;
sio:SIO_000772
miriam-pubmed:16364894
;
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:NP169550.RAgkVfij4mK-xZUqDoIoVS2HguM5tUZU_1Rwaox1rmjO0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}