@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ
> .
@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:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_head
{
this:
np:hasAssertion
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion
;
np:hasProvenance
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion
a
np:Assertion
.
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_provenance
a
np:Provenance
.
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN999703cd6c69df2042bfaaea29cb1c82
sio:SIO_000628
miriam-gene:3630
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_provenance
{
dgn-np:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_assertion
dcterms:description
"[The mechanisms through which hypertension contributes to the occurrence of myocardial infarction should be discussed from two points of view: (1) common risk factors for the two diseases, such as genetic risk, insulin resistance, sympathetic hyperactivity, and vasoactive substances such as angiotensin K, and (2) linking factors that are induced by hypertension and contribute to the development of atherosclerosis and myocardial infarction, such as atherosclerosis 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:8677859
;
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:NP239081.RAH9lOUx-uL3QjV5XiG_VawOCPWZCCgXuBhw0NZHmEYOQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}