@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_provenance
;
np:hasPublicationInfo
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_assertion
a
np:Assertion
.
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_provenance
a
np:Provenance
.
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_assertion
{
miriam-gene:1605
a
ncit:C16612
.
lld:C0686353
a
ncit:C7057
.
dgn-gda:DGN16c9eb563fd6a693f31bc6989bdb8b6e
sio:SIO_000628
miriam-gene:1605
,
lld:C0686353
;
a
sio:SIO_001121
.
}
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_provenance
{
dgn-np:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_assertion
dcterms:description
"[Not all of the limb girdle muscular dystrophies have been identified in molecular terms and, as yet, no disorder has been associated with mutations of the syntrophin or the dystroglycan genes.]. 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:8894415
;
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:NP711839.RALXJn_f87rClRX81ac3zo81IFWqhaneDukqcl-txIQVM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}