@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A
> .
@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:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_head
{
this:
np:hasAssertion
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_assertion
;
np:hasProvenance
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_provenance
;
np:hasPublicationInfo
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_assertion
a
np:Assertion
.
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_provenance
a
np:Provenance
.
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_assertion
{
miriam-gene:6445
a
ncit:C16612
.
lld:C0686353
a
ncit:C7057
.
dgn-gda:DGNa1b568024b27e20ebf6a72727932599f
sio:SIO_000628
miriam-gene:6445
,
lld:C0686353
;
a
sio:SIO_001121
.
}
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_provenance
{
dgn-np:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_assertion
dcterms:description
"[The relatively high frequency of SGP among Brazilian people with LGMD may be due to the disproportionally high frequency of African Brazilian SGP patients with the same mutation (particularly among LGMD2C and 2F patients), suggesting a founder effect.]. 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:10385046
;
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:NP460086.RAmY3_odmFVDGSvZJ73qX6zb446sUf0SiHWuyv13RJt0A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}