@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_head
{
this:
np:hasAssertion
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_assertion
;
np:hasProvenance
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_provenance
;
np:hasPublicationInfo
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_assertion
a
np:Assertion
.
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_provenance
a
np:Provenance
.
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_assertion
{
miriam-gene:178
a
ncit:C16612
.
lld:C0017919
a
ncit:C7057
.
dgn-gda:DGN104dd4cbdfb700657685ef2e87847e38
sio:SIO_000628
miriam-gene:178
,
lld:C0017919
;
a
sio:SIO_001121
.
}
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_provenance
{
dgn-np:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_assertion
dcterms:description
"[Glycogen Storage Disease Type III (limit dextrinosis; Cori or Forbes disease) is an autosomal recessive disorder of glycogen metabolism caused by deficient activity of glycogen debranching enzyme in liver and muscle (Glycogen Storage Disease Type IIIa) or liver only (Glycogen Storage Disease Type IIIb).]. 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:20648714
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP827442.RALNNrZvfAfqlfHvh_pr83uf5LmaFVb6u8yQa8zt_f3tw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:00+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}