@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE
> .
@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/v3.0.0/void/
> .
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_head
{
this:
np:hasAssertion
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_assertion
;
np:hasProvenance
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_assertion
a
np:Assertion
.
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_provenance
a
np:Provenance
.
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0410226
a
ncit:C7057
.
dgn-gda:DGN1095f3aa21c790d0862d1259a7322c9d
sio:SIO_000628
miriam-gene:2837
,
lld:C0410226
;
a
sio:SIO_001121
.
}
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_provenance
{
dgn-np:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_assertion
dcterms:description
"[Myotonic Dystrophy type I (DM1) is caused by an abnormal expansion of CTG triplets in the 3' UTR of the dystrophia myotonica protein kinase (DMPK) gene, leading to the aggregation of the mutant transcript in nuclear RNA foci.]. 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:22156369
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP432374.RATRpVi4ehZKEFG82ObNOVfP6p42oGNWE2_trGb6_rpGE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:52+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}