@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY
> .
@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:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_head
{
this:
np:hasAssertion
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_assertion
;
np:hasProvenance
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_provenance
;
np:hasPublicationInfo
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_assertion
a
np:Assertion
.
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_provenance
a
np:Provenance
.
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0391957
a
ncit:C7057
.
dgn-gda:DGN2ca46ea20cbfba4db23259cfb792a3e9
sio:SIO_000628
miriam-gene:3126
,
lld:C0391957
;
a
sio:SIO_001121
.
}
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_provenance
{
dgn-np:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_assertion
dcterms:description
"[This finding, together with the low HLA-A9 gene frequency in our group of normal Egyptians as compared with other ethnic populations, strongly suggests an association between antigen A9 and one or more of the polygenes controlling the development of idiopathic 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:3971947
;
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:NP663917.RAvqDv-TfkdhKjNqfytb9nxsc1rOQ7t87XgDVJGe6MuCY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:41+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" .
}