@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM
> .
@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:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_head
{
this:
np:hasAssertion
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_assertion
;
np:hasProvenance
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_assertion
a
np:Assertion
.
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_provenance
a
np:Provenance
.
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN3a7a40f746251dcb38caa01d45a5ea70
sio:SIO_000628
miriam-gene:1636
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_provenance
{
dgn-np:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_assertion
dcterms:description
"[The homozygous deletion allele (DD) of the angiotensin-I converting enzyme (ACE) gene and the T235 homozygote of the angiotensinogen (AGT) gene have been reported to be correlated with an increased prevalence of coronary artery disease (CAD) and myocardial infarction (MI).]. 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:9254851
;
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:NP1378361.RAEgFb48CciPH2IfbgM0rM6RfgBMqvIWBR_K_HdfgpthM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:10+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" .
}