@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_head
{
this:
np:hasAssertion
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_assertion
;
np:hasProvenance
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_assertion
a
np:Assertion
.
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_provenance
a
np:Provenance
.
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN22c95edf8bda954c592108ea5b701c87
sio:SIO_000628
miriam-gene:3630
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_provenance
{
dgn-np:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_assertion
dcterms:description
"[Claiming that the result of genotyping predicts optimal treatment in certain epilepsies is equivalent to stating that genotyping for diabetes has become available and that, based on this breakthrough, insulin can now be selected as the treatment of choice in those who test positive.]. 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:19087113
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP709586.RAlMsQZAuMUQY-sQX9_muWqgJvL4XpFdzZ7ELiuq1VMjQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:06+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}