@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc
> .
@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:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_head
{
this:
np:hasAssertion
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_assertion
;
np:hasProvenance
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_provenance
;
np:hasPublicationInfo
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_assertion
a
np:Assertion
.
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_provenance
a
np:Provenance
.
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0393570
a
ncit:C7057
.
dgn-gda:DGNafa84173c65f4dc00625da7fddc0f4af
sio:SIO_000628
miriam-gene:4137
,
lld:C0393570
;
a
sio:SIO_001121
.
}
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_provenance
{
dgn-np:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_assertion
dcterms:description
"[They include the largely sporadic Alzheimer's disease, progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), Pick's disease (PiD), argyrophilic grain disease, as well as the inherited frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).]. 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:15036206
;
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:NP436624.RAv2F-TOewVtV438K929qV1FnVIoP7HVVSffneFUifJEc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:03+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" .
}