@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8
> .
@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:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_head
{
this:
np:hasAssertion
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_assertion
;
np:hasProvenance
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_assertion
a
np:Assertion
.
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_provenance
a
np:Provenance
.
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_assertion
{
miriam-gene:7098
a
ncit:C16612
.
lld:C0276226
a
ncit:C7057
.
dgn-gda:DGN5329d673a6b8391ce5b448c6df383546
sio:SIO_000628
miriam-gene:7098
,
lld:C0276226
;
a
sio:SIO_001121
.
}
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_provenance
{
dgn-np:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_assertion
dcterms:description
"[Finally, mutations in UNC93B1 and TLR3 are associated with childhood herpes simplex encephalitis, which strikes only once in most patients, with almost no recorded cases of more than two bouts of this 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:20236864
;
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:NP487484.RA5JiU5g9hRh14YAqKWqZ3vCAunfAqqKK2QzlMFIPeSH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}