@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo
> .
@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:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_head
{
this:
np:hasAssertion
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_assertion
;
np:hasProvenance
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_provenance
;
np:hasPublicationInfo
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_assertion
a
np:Assertion
.
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_provenance
a
np:Provenance
.
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_assertion
{
miriam-gene:7031
a
ncit:C16612
.
lld:C0276496
a
ncit:C7057
.
dgn-gda:DGNc4d61133c2a152185a94cf8e9d02437f
sio:SIO_000628
miriam-gene:7031
,
lld:C0276496
;
a
sio:SIO_001121
.
}
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_provenance
{
dgn-np:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_assertion
dcterms:description
"[Eleven early-onset dementia families, all with affected individuals who have either presented clinical symptoms of early onset familial Alzheimer's disease (EOFAD) or have been confirmed to have EOFAD by autopsy, and two early onset cases with biopsy-confirmed AD pathology, were screened for missense mutations in the entire coding region of presenilin-1 (PS-1) and -2 (PS-2) genes.]. 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:9172170
;
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:NP194380.RAvkKm7Ln_8SGasZdi7R2p9g6wkho16L1osouX1rsJdWo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}