@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c
> .
@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:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_head
{
this:
np:hasAssertion
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_assertion
;
np:hasProvenance
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_assertion
a
np:Assertion
.
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_provenance
a
np:Provenance
.
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_assertion
{
miriam-gene:4035
a
ncit:C16612
.
lld:C0011268
a
ncit:C7057
.
dgn-gda:DGN90b3fdfcae9a15435ecfa78e699456c1
sio:SIO_000628
miriam-gene:4035
,
lld:C0011268
;
a
sio:SIO_001121
.
}
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_provenance
{
dgn-np:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_assertion
dcterms:description
"[Using a biallelic genetic marker in exon 3 of LRP, late-onset AD cases markedly differed from the control subjects in the distribution of LRP genotypes, and this difference was highly accentuated among AD cases with positive family history of senile dementia.]. 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:9222170
;
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:NP765787.RAYMQrjWFqOoib-8nG9FkT8B2I3igwDMlJzU4_37HNQ_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}