@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_head
{
this:
np:hasAssertion
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_assertion
;
np:hasProvenance
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_provenance
;
np:hasPublicationInfo
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_assertion
a
np:Assertion
.
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_provenance
a
np:Provenance
.
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN7348784b7fc1ecb28873a73a7c8d6dc2
sio:SIO_000628
miriam-gene:5621
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_provenance
{
dgn-np:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_assertion
dcterms:description
"[We conducted a case-control study to compare the PRNP codon 129 genotype distribution in Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), and primary progressive aphasia (PPA), including 281 AD, 256 ALS, 39 PPA, and 415 healthy control subjects.]. 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:16315279
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP824048.RA1HSHWt-OZLgfDQRi4Tw3RQgWsEV9X6vszykmOInYVKM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}