@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g
> .
@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:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_head
{
this:
np:hasAssertion
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_assertion
;
np:hasProvenance
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_provenance
;
np:hasPublicationInfo
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_assertion
a
np:Assertion
.
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_provenance
a
np:Provenance
.
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_assertion
{
miriam-gene:1476
a
ncit:C16612
.
lld:C0027066
a
ncit:C7057
.
dgn-gda:DGNd76c945b10ab2f191e98aba105b54678
sio:SIO_000628
miriam-gene:1476
,
lld:C0027066
;
a
sio:SIO_001121
.
}
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_provenance
{
dgn-np:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_assertion
dcterms:description
"[Linkage analyses have shown that the genes for both these forms of myoclonus are closely linked to 21q22.3 DNA markers, suggesting that they are caused by mutations at the same locus (EPM1).]. 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:9153533
;
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:NP617499.RAgJ4IMPmpgD3mnICl3pah8CrE4672KGGUKaVl8QyYk7g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}