@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c
> .
@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:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_head
{
this:
np:hasAssertion
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_assertion
;
np:hasProvenance
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_provenance
;
np:hasPublicationInfo
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_assertion
a
np:Assertion
.
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_provenance
a
np:Provenance
.
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_assertion
{
miriam-gene:7031
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN320ddcaa8b882f514aa89007b39be686
sio:SIO_000628
miriam-gene:7031
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_provenance
{
dgn-np:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_assertion
dcterms:description
"[Most of early-onset forms of Alzheimer's disease (AD) are caused by inherited mutations located on chromosomes 14 and 1, the gene products of which have been recently identified and referred to as presenilins 1 (PS1) and 2 (PS2), respectively.]. 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:10495106
;
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:NP178858.RAwlsQoQ_98N_XwPOaO0wGUNmBE1-H27TUHRnTv5ANL1c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}