@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g
> .
@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:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_head
{
this:
np:hasAssertion
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_assertion
;
np:hasProvenance
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_assertion
a
np:Assertion
.
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_provenance
a
np:Provenance
.
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_assertion
{
miriam-gene:5256
a
ncit:C16612
.
lld:C0029438
a
ncit:C7057
.
dgn-gda:DGN3ea7b9dee289745ec4276046fda11806
sio:SIO_000628
miriam-gene:5256
,
lld:C0029438
;
a
sio:SIO_001121
.
}
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_provenance
{
dgn-np:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_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:NP606871.RAbkjK0tb_IEDCF_XtJcR7YqNbH4uv6vR6EvZE_9BDE_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}