@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w
> .
@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:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_head
{
this:
np:hasAssertion
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion
;
np:hasProvenance
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_provenance
;
np:hasPublicationInfo
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion
a
np:Assertion
.
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_provenance
a
np:Provenance
.
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNbf38e51368725be0edfec43fb4b0e5d9
sio:SIO_000628
miriam-gene:3643
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_provenance
{
dgn-np:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_assertion
dcterms:description
"[To determine whether a microsatellite polymorphism of the insulin receptor gene (INSR) is associated with essential hypertension, as has been demonstrated previously for an RsaI restriction fragment length polymorphism (RFLP), and to examine blood pressure and plasma lipid profiles in relation to genotype.]. 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:7769500
;
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:NP331672.RABfWQFG5KcayibK4dKtjdIL30-3xeDwVNsQZfD6uv92w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}