@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_assertion
;
np:hasProvenance
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_assertion
a
np:Assertion
.
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_provenance
a
np:Provenance
.
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_assertion
{
miriam-gene:1476
a
ncit:C16612
.
lld:C0751783
a
ncit:C7057
.
dgn-gda:DGN630acb6b02ee456f0b9f1c4958fb8220
sio:SIO_000628
miriam-gene:1476
,
lld:C0751783
;
a
sio:SIO_001121
.
}
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_provenance
{
dgn-np:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_assertion
dcterms:description
"[Using three highly polymorphic DNA markers (D21S212, PFKL, and D21S171) which flank the EPM1 locus, we performed linkage analysis to investigate whether or not the EPM1 gene is also implicated in Lafora disease.]. 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:7485240
;
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:NP628845.RAWpfASqa138Wroam5h0b7JlhBXZaqcjgbxy6aFMQDQLc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}