@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_head
{
this:
np:hasAssertion
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion
;
np:hasProvenance
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion
a
np:Assertion
.
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_provenance
a
np:Provenance
.
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGN8a818fa50326e343e4926aee38ba9751
sio:SIO_000628
miriam-gene:1636
,
lld:C0878544
;
a
sio:SIO_001121
.
}
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_provenance
{
dgn-np:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_assertion
dcterms:description
"[Recent reports have shown that the frequency of the homozygous deletion genotype (DD) of the angiotensin-converting enzyme (ACE) gene is highly associated with myocardial infarction and cardiomyopathy, particularly in those considered to be at low risk for coronary heart disease (CHD) on the basis of their apoB or LDL cholesterol concentrations.]. 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:7773733
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1321383.RARC_DgDY1YBwinWXGJ11hfA-lLIH2sTKv7Gplq8Q6awM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:45+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}