@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg
> .
@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:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_head
{
this:
np:hasAssertion
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_assertion
;
np:hasProvenance
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_provenance
;
np:hasPublicationInfo
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_assertion
a
np:Assertion
.
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_provenance
a
np:Provenance
.
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_assertion
{
miriam-gene:23209
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN04f6b2777845e6c955deac375815643e
sio:SIO_000628
miriam-gene:23209
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_provenance
{
dgn-np:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_assertion
dcterms:description
"[To examine the influence of genetic susceptibility to essential hypertension (EH) and the genetic susceptibility to premature myocardial infarction (MI) on longitudinal development of systolic blood pressure (SBP) and left ventricular mass (LVM) in youth.]. 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:12777557
;
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:NP242129.RAvZrxbDE0oAXZZ9KJxS7oPLsYJ4GHQa1LAsQMAldPswg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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" .
}