@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw
> .
@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:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_head
{
this:
np:hasAssertion
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_assertion
;
np:hasProvenance
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_provenance
;
np:hasPublicationInfo
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_assertion
a
np:Assertion
.
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_provenance
a
np:Provenance
.
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_assertion
{
miriam-gene:6638
a
ncit:C16612
.
lld:C1285162
a
ncit:C7057
.
dgn-gda:DGN9c73d2043efa38ef11a8167ab9c0c8b7
sio:SIO_000628
miriam-gene:6638
,
lld:C1285162
;
a
sio:SIO_001121
.
}
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_provenance
{
dgn-np:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_assertion
dcterms:description
"[Reduction of the survival of motor neurons (SMN) protein levels causes the motor neuron degenerative disease spinal muscular atrophy, the severity of which correlates with the extent of reduction in SMN.]. 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:15964810
;
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:NP766146.RAY0EzKDTQ_zURNYCFHceqPL_zsMsXVaLCI-OQjSx5wjw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}