@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo
> .
@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:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_head
{
this:
np:hasAssertion
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_assertion
;
np:hasProvenance
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_provenance
;
np:hasPublicationInfo
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_assertion
a
np:Assertion
.
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_provenance
a
np:Provenance
.
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_assertion
{
miriam-gene:1760
a
ncit:C16612
.
lld:C0027126
a
ncit:C7057
.
dgn-gda:DGN52f1dd74c778e017f9728d8dde342944
sio:SIO_000628
miriam-gene:1760
,
lld:C0027126
;
a
sio:SIO_001121
.
}
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_provenance
{
dgn-np:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_assertion
dcterms:description
"[This second form of myotonic dystrophy may help resolve the confusion that remains about how the CTG repeat expansion in the 3' untranslated portion of the myotonin protein kinase gene causes the multisystem involvement of DM.]. 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:10063831
;
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:NP246878.RAqKKj7BrVyhlC19xDQB7OpJU2vYgUk2HflhNUyYwskjo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:38+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" .
}