@prefix bfo: <
http://purl.obolibrary.org/obo/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U
> .
@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 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:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_head
{
this:
np:hasAssertion
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_assertion
;
np:hasProvenance
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_provenance
;
np:hasPublicationInfo
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_assertion
a
np:Assertion
.
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_provenance
a
np:Provenance
.
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGNff8be8a3cd348b339edc04c7433d6dac
sio:SIO_000628
miriam-gene:5663
,
lld:C0085400
;
a
sio:SIO_001122
.
}
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_provenance
{
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_assertion
dcterms:description
"[Some of the PS1 mutations studied (M139V, I143F, G209V, R269H, E280A), but not others, were also associated with faster rates of NFT formation and accelerated neuronal loss in the majority of the patients who harboured them when compared with sporadic Alzheimer's disease patients.]. 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:10468510
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
bfo:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
xsd:date
.
dgn-void:source_evidence_literature
a
bfo:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP261618.RAFTD5r7yDkO4-Qy6uV1Jq4gAkoNcGCKyBq1QcedRTD6U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:44+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" .
}