@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE
> .
@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:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_head
{
this:
np:hasAssertion
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_assertion
;
np:hasProvenance
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_assertion
a
np:Assertion
.
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_provenance
a
np:Provenance
.
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_assertion
{
miriam-gene:5211
a
ncit:C16612
.
lld:C0751785
a
ncit:C7057
.
dgn-gda:DGN52ea0e3431578accc3a9a97f6ff3536f
sio:SIO_000628
miriam-gene:5211
,
lld:C0751785
;
a
sio:SIO_001121
.
}
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_provenance
{
dgn-np:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_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:NP884114.RA3GvzWBzMcOhG1Y4q7Al2t4WNeW24eDunVje1JVh8JWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}