@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio
> .
@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:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_head
{
this:
np:hasAssertion
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_assertion
;
np:hasProvenance
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_provenance
;
np:hasPublicationInfo
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_assertion
a
np:Assertion
.
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_provenance
a
np:Provenance
.
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_assertion
{
miriam-gene:1760
a
ncit:C16612
.
lld:C1883552
a
ncit:C7057
.
dgn-gda:DGN92d03084a00a28b8bf1af48a9880fdd2
sio:SIO_000628
miriam-gene:1760
,
lld:C1883552
;
a
sio:SIO_001121
.
}
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_provenance
{
dgn-np:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_assertion
dcterms:description
"[The disorder, characterized by myotonia, muscle wasting and weakness, cataract, insulin resistance, and mental impairment, is caused by the expansion of an unstable CTG repeat located in the 3' untranslated region of DMPK.]. 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:11978764
;
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:NP298709.RADGQS1K-DWfqHGPmvWYP8Tg3cbWtOMQQtmhiM8kXYWio130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}