@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw
> .
@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:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_head
{
this:
np:hasAssertion
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_assertion
;
np:hasProvenance
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_assertion
a
np:Assertion
.
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_provenance
a
np:Provenance
.
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_assertion
{
miriam-gene:4043
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNbe28e2f1867be2d5b0c851d064521c22
sio:SIO_000628
miriam-gene:4043
,
lld:C0002395
;
a
sio:SIO_001122
.
}
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_provenance
{
dgn-np:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_assertion
dcterms:description
"[According to our data, the variation at the LRPAP1 gene is associated with the risk of developing LOAD. This is in agreement with the role of the LRPAP1 protein in the amyloidogenic pathway.]. 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:11425005
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55186.RAT5QZQU72iqxCCtZr8h4Q0rHo0nUvrorlogy1b6aNkhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}