@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8
> .
@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:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_head
{
this:
np:hasAssertion
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_assertion
;
np:hasProvenance
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_provenance
;
np:hasPublicationInfo
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_assertion
a
np:Assertion
.
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_provenance
a
np:Provenance
.
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_publicationInfo
a
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.
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dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0494463
a
ncit:C7057
.
dgn-gda:DGN624f418f4023a3859326d28c6d0a5c77
sio:SIO_000628
miriam-gene:5663
,
lld:C0494463
;
a
sio:SIO_001121
.
}
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_provenance
{
dgn-np:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_assertion
dcterms:description
"[In a series of sibpairs with late onset Alzheimer's disease, we have examined the segregation of the loci involved in the early onset, autosomal dominant form of the disorder by using flanking microsatellite repeat markers: thus we have used APP-PCR3 and D21S210 to examine the segregation of the amyloid-beta precursor protein (APP) gene, the markers DI 4S77 and D14S284 to examine the segregation of the presenilin 1 (PSI) gene and the markers D1S227, D1S249 and D1S419 to examine the segregation of presenilin 2 (PS2).]. 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:10430506
;
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:NP292665.RAXQSCV9UMitY2rfVv7jR_UbMnAkZeSvxdADcnlWaM3t8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}