@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ
> .
@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:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_head
{
this:
np:hasAssertion
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_assertion
;
np:hasProvenance
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_assertion
a
np:Assertion
.
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_provenance
a
np:Provenance
.
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN1859b2da1f0d2c97e0cf43dbfbd86437
sio:SIO_000628
miriam-gene:1437
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_provenance
{
dgn-np:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_assertion
dcterms:description
"[This report describes the relationships between tau markers in the cerebrospinal fluid (CSF), the degree of cognitive impairment and the predictive value of genetic markers such the alleles of apolipoprotein E, namely, the presence of Apo-epsilon4, as part of a longitudinal study.]. 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:16099324
;
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:NP434774.RA3TnxxNUmqXetT_fqrtw1lN9zt44QvqTghHmx0lxxnUQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}