@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY
> .
@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:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_head
{
this:
np:hasAssertion
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_assertion
;
np:hasProvenance
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_provenance
;
np:hasPublicationInfo
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_assertion
a
np:Assertion
.
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_provenance
a
np:Provenance
.
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_assertion
{
miriam-gene:5786
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGN815e90d3f99b2941ffb3bd5ee669bd5c
sio:SIO_000628
miriam-gene:5786
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_provenance
{
dgn-np:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_assertion
dcterms:description
"[The concordance of NP and NFT pathological change and the discordance of LRP support the concept that, in AD, the former are primarily under genetic control whereas the latter (LRP) is more influenced by disease duration and environmental factors.]. 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:17615170
;
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:NP263420.RAX7rjvRXCKsmZ0WEFQj4q4J5G55MHwUoWLH7xtVQKKhY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}