@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k
> .
@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/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_assertion
a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_publicationInfo
a
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.
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dgn-np:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGNc9d6631ad7bf12f829b5682962c2ef38
sio:SIO_000628
miriam-gene:348
,
lld:C0524851
;
a
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.
}
dgn-np:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_provenance
{
dgn-np:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_assertion
dcterms:description
"[Herein, we have expanded the study group to 19 AD patients homozygous for APOE4 or APOE3, as well as 30 patients with other neurodegenerative diseases, including diffuse Lewy body disease, Pick's disease, progressive supranuclear palsy, Parkinson's disease, and human immunodeficiency virus-1 encephalitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:9258256
;
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:NP1378587.RALNWBWONIAYmxiAwsAOvCO6Mdmc4RNhQSke95Pqraz_k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:10+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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" .
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pav:version
"v4.0.0" .
}