@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0
> .
@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:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_head
{
this:
np:hasAssertion
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_assertion
;
np:hasProvenance
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_provenance
;
np:hasPublicationInfo
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_assertion
a
np:Assertion
.
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_provenance
a
np:Provenance
.
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C1392786
a
ncit:C7057
.
dgn-gda:DGNbf11a6a8231ec93e0a33c878b6225713
sio:SIO_000628
miriam-gene:348
,
lld:C1392786
;
a
sio:SIO_001121
.
}
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_provenance
{
dgn-np:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_assertion
dcterms:description
"[Identification of biological or cognitive changes in brain function, associated with allelic variation in Apolipoprotein E, is important for unravelling the mechanism behind the increased risk for Alzheimer's disease associated with the varepsilon4 allele.]. 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:15925117
;
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:NP392250.RAJDoVP2hXo-2VlQAjijjbMhhQn6C5aafMZ7YIjuXIcC0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}