@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc
> .
@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:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_head
{
this:
np:hasAssertion
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion
;
np:hasProvenance
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion
a
np:Assertion
.
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_provenance
a
np:Provenance
.
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN8412940f9981e9b4843fbefa06acf3ed
sio:SIO_000628
miriam-gene:183
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_provenance
{
dgn-np:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_assertion
dcterms:description
"[Exciting new discoveries concerned with polymorphisms of genes coding for angiotensin converting enzyme (ACE) and angiotensinogen suggest that Ang II may be genetically associated with increased risk for myocardial infarction, hypertension and left ventricular hypertrophy.]. 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:8583476
;
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:NP191009.RAbn6JB8jdT1r9aS6vO7d1IlkO_v7Zr-rlq8Vru8SxdTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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: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" .
}