@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM
> .
@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:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_assertion
;
np:hasProvenance
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_provenance
;
np:hasPublicationInfo
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_assertion
a
np:Assertion
.
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_provenance
a
np:Provenance
.
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_assertion
{
miriam-gene:3497
a
ncit:C16612
.
lld:C0014553
a
ncit:C7057
.
dgn-gda:DGNa8ef7c999a2056fc89b2a753bfb43c95
sio:SIO_000628
miriam-gene:3497
,
lld:C0014553
;
a
sio:SIO_001121
.
}
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_provenance
{
dgn-np:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_assertion
dcterms:description
"[Our present linkage study tested the hypothesis that DNA sequence variants associated with the gene encoding the neural cell adhesion molecule (NCAM) confer genetic susceptibility to IGE traits in 57 families ascertained through patients with either juvenile myoclonic epilepsy, juvenile or childhood absence epilepsy.]. 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:8884172
;
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:NP842500.RAGqzkFJ6N17xAxIcdGyFRi5kXU7_1Bbuz6ifVWv4DnOM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}