@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE
> .
@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:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_head
{
this:
np:hasAssertion
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion
;
np:hasProvenance
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion
a
np:Assertion
.
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_provenance
a
np:Provenance
.
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGNe9a0d0ef270f6d8d3623e778e0546fa0
sio:SIO_000628
miriam-gene:348
,
lld:C0497327
;
a
sio:SIO_001121
.
}
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_provenance
{
dgn-np:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_assertion
dcterms:description
"[We suggest that the lower frequency of dementia in the Amish may be partially explained by the decreased frequency of the APOE-4 allele in this population, and that the inbred nature of this pedigree, with its strong clustering of cases contrasted against the lower frequency of dementia, indicates that additional genetic factors influence late-onset 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:8651641
;
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:NP1351203.RA4iWg5YlXEX8w_qXFVN2x891e86xWMmFlRwhfCse6VKE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:58+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" .
}