@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts
> .
@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:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_head
{
this:
np:hasAssertion
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_assertion
;
np:hasProvenance
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_provenance
;
np:hasPublicationInfo
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_assertion
a
np:Assertion
.
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_provenance
a
np:Provenance
.
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_assertion
{
miriam-gene:1760
a
ncit:C16612
.
lld:C0559758
a
ncit:C7057
.
dgn-gda:DGNf48c6e3952bc32bd34eb8f06dacbbf49
sio:SIO_000628
miriam-gene:1760
,
lld:C0559758
;
a
sio:SIO_001121
.
}
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_provenance
{
dgn-np:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_assertion
dcterms:description
"[It is quite important to know the exact localization and function of myotonin protein kinase (MtPK), identified as the gene product of myotonic dystrophy, the most prevalent disease with multisystem disorders among muscular dystrophies.]. 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:9094985
;
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:NP927195.RATVbUYH73hLFeaTDK3m2kyI__OUF3HyQH6ry3YoqqLts130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}