@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE
> .
@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:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_head
{
this:
np:hasAssertion
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_assertion
;
np:hasProvenance
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_assertion
a
np:Assertion
.
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_provenance
a
np:Provenance
.
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_assertion
{
miriam-gene:5664
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN7b7836a3f20545720f266b0b63107057
sio:SIO_000628
miriam-gene:5664
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_provenance
{
dgn-np:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_assertion
dcterms:description
"[Because 50% of AD cases have no APOE epsilon4 alleles and families showing mendelian inheritance of AD exist in whom there are no mutations in any of the APP, PS1, or PS2 genes, it is likely that there are additional AD risk factors, both genetic and environmental, still to be identified.]. 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:9052714
;
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:NP1368441.RAiHJAbdV1kqCiKbXQ3q60CvA4HDrRTskvPxxzaEn69cE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:06+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" .
}