@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM
> .
@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:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_head
{
this:
np:hasAssertion
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_assertion
;
np:hasProvenance
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_provenance
;
np:hasPublicationInfo
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_assertion
a
np:Assertion
.
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_provenance
a
np:Provenance
.
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN2aba173fcbf2dff1d249c5f14177af86
sio:SIO_000628
miriam-gene:1636
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_provenance
{
dgn-np:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_assertion
dcterms:description
"[In a study of 261 patients with Alzheimer disease (AD) and 306 cognitively normal control subjects from Germany, Switzerland, and Italy, we found no association between genotype counts or allelic frequencies of DCP1, the gene encoding angiotensin-converting enzyme.]. 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:11992568
;
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:NP161698.RA_zajv3LAIxBjwuDI6i9w1O7RLLjeFv7CJqy1SY751YM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}