@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg
> .
@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:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_head
{
this:
np:hasAssertion
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_assertion
;
np:hasProvenance
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_provenance
;
np:hasPublicationInfo
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_assertion
a
np:Assertion
.
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_provenance
a
np:Provenance
.
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_assertion
{
miriam-gene:5256
a
ncit:C16612
.
lld:C0017495
a
ncit:C7057
.
dgn-gda:DGN3e89c3f1c4b55b4f33be5a4c89110b4f
sio:SIO_000628
miriam-gene:5256
,
lld:C0017495
;
a
sio:SIO_001121
.
}
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_provenance
{
dgn-np:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_assertion
dcterms:description
"[The diagnosis of glycogen storage disease (GSD) type IX is often complicated by the complexity of the phosphorylase kinase enzyme (PHK), and molecular analysis is the preferred way to provide definitive diagnosis.]. 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:21131218
;
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:NP778389.RAyZ0aX06n9gHwrNJGkfAI1WpAUY4aTpWzuJ7z9uhIVdg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}