@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18
> .
@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:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_head
{
this:
np:hasAssertion
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion
;
np:hasProvenance
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_provenance
;
np:hasPublicationInfo
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion
a
np:Assertion
.
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_provenance
a
np:Provenance
.
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGNcb04f84eb28b38fb9b634b7d32527be8
sio:SIO_000628
miriam-gene:4137
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_provenance
{
dgn-np:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_assertion
dcterms:description
"[The polymorphism of apolipoprotein E (apoE) has been recognized as a genetic risk factor in different neurodegenerative disorders, with or without tau protein- related neuropathology, but few published epidemiological data are available as concerns the association of different apoE alleles with two relatively rare forms of dementia, Pick's disease (PiD) and Huntington's disease (HD).]. 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:10924769
;
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:NP290735.RAQ1kl9cZPIdloqkmWlxaIsaTBSkg4bRt2dfOj1jAca18130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:57+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" .
}