@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U
> .
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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:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_assertion
a
np:Assertion
.
dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_provenance
a
np:Provenance
.
dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_assertion
{
miriam-gene:3416
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN0c42de23159e49f19c2fef082fe7120b
sio:SIO_000628
miriam-gene:3416
,
lld:C0002395
;
a
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.
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dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_provenance
{
dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_assertion
dcterms:description
"[Genotyping of single nucleotide polymorphisms (SNPs) in the IDE gene in Finnish patients with AD and controls revealed SNPs rs4646953 and rs4646955 to be associated with AD, conferring an approximately two-fold increased risk.]. 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:17496198
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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 .
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dgn-np:NP57134.RAUL_3FdKUHr1vnb_rFrm-FA5SLlPRcvDnx6UYdnIrY9U130_publicationInfo
{
this:
dcterms:created
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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
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pav:authoredBy
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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