@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q
> .
@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:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_assertion
a
np:Assertion
.
dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_provenance
a
np:Provenance
.
dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_assertion
{
miriam-gene:3077
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNdf4884e35647593aa1cebe4422a47b66
sio:SIO_000628
miriam-gene:3077
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_provenance
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dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_assertion
dcterms:description
"[In a population-based cohort study, including 268 incident AD patients and 2079 control individuals, we investigated the influence of the HFE C282Y and H63D variants and the apolipoprotein E4 (APOE epsilon 4) allele on the incidence, and age at onset of AD.]. 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:17628213
;
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 .
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dgn-np:NP279943.RAUKvp73NuFo0FiUCT0m0uYOOIvbZA505sC1yThdxy37Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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
> , <
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> , <
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
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