@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs
> .
@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:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_head
{
this:
np:hasAssertion
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_assertion
;
np:hasProvenance
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_assertion
a
np:Assertion
.
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_provenance
a
np:Provenance
.
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_assertion
{
miriam-gene:2641
a
ncit:C16612
.
lld:C0017925
a
ncit:C7057
.
dgn-gda:DGNb2568a2aa70bad7939cc469fc1d0273f
sio:SIO_000628
miriam-gene:2641
,
lld:C0017925
;
a
sio:SIO_001121
.
}
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_provenance
{
dgn-np:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_assertion
dcterms:description
"[Human liver glycogen phosphorylase deficiency, also known as glycogen storage disease type VI (GSD VI) or Hers disease, is characterized by hepatomegaly and reduced or absent glycogenolytic response to the injection of glucagon.]. 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:2883891
;
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:NP812320.RArTCd7pFtX6U4_DUa9c78TEDdbONRLa1WUyIn3ZKAgKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}