@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro
> .
@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:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_head
{
this:
np:hasAssertion
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_assertion
;
np:hasProvenance
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_provenance
;
np:hasPublicationInfo
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_assertion
a
np:Assertion
.
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_provenance
a
np:Provenance
.
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_assertion
{
miriam-gene:6606
a
ncit:C16612
.
lld:C0151514
a
ncit:C7057
.
dgn-gda:DGN492211768ca3ff070a208f743a6b17be
sio:SIO_000628
miriam-gene:6606
,
lld:C0151514
;
a
sio:SIO_001121
.
}
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_provenance
{
dgn-np:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_assertion
dcterms:description
"[Notably, SMN deficiency in SMA leads to the aberrant subcellular localization of Gemin8 and PP1γ in the atrophic skeletal muscles, suggesting that the function of PP1γ is likely to be affected in disease.]. 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:22454514
;
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:NP672443.RAoL9xP6IsdntWFKym-Q62jBCeiJB_QEckvMkTo1CBpro130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}