@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U
> .
@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:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_head
{
this:
np:hasAssertion
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_assertion
;
np:hasProvenance
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_provenance
;
np:hasPublicationInfo
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_assertion
a
np:Assertion
.
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_provenance
a
np:Provenance
.
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_assertion
{
miriam-gene:9211
a
ncit:C16612
.
lld:C2931469
a
ncit:C7057
.
dgn-gda:DGN3069379a9841543d166ff3d9c2ab7900
sio:SIO_000628
miriam-gene:9211
,
lld:C2931469
;
a
sio:SIO_001121
.
}
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_provenance
{
dgn-np:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_assertion
dcterms:description
"[In families with autosomal dominant partial epilepsy with auditory features (ADPEAF) with mutations in the LGI1 gene, we evaluated clustering of mutations within the gene and associations of penetrance and phenotypic features with mutation location and predicted effect (truncation or missense).]. 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:22323750
;
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:NP371450.RAd0xYfNGrtuLRk-by4PLuB8bd_EI1_NnHFSOObVFod4U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}