@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4
> .
@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:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_head
{
this:
np:hasAssertion
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_assertion
;
np:hasProvenance
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_assertion
a
np:Assertion
.
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_provenance
a
np:Provenance
.
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_assertion
{
miriam-gene:10531
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNbae9508cc65e7dbcea04101b35617a93
sio:SIO_000628
miriam-gene:10531
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_provenance
{
dgn-np:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_assertion
dcterms:description
"[We investigated if there is an increased susceptibility to AD, which can be attributed to genetic variation in the hPreP gene PITRM1 and if the proteolytic efficiency of recombinant hPreP variants is affected.]. 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:19962426
;
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:NP354730.RAsGhvZNrv-MBp6wDG4Z7Md2EwxGj0hlxpyioMgazsqT4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}