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http://rdf.disgenet.org/nanopublications.trig#NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I
> .
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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:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_head
{
this:
np:hasAssertion
dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_assertion
;
np:hasProvenance
dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_provenance
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dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_assertion
a
np:Assertion
.
dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_provenance
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np:Provenance
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dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_publicationInfo
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{
miriam-gene:3949
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN8297f93b65dd412085be49261867c8c2
sio:SIO_000628
miriam-gene:3949
,
lld:C0085580
;
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.
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dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_provenance
{
dgn-np:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_assertion
dcterms:description
"[The present study examined genotypes for the obesity-associated ApaLI restriction fragment length polymorphism of LDLR, and genotypes for a hypertension-associated RsaI restriction fragment length polymorphism at the insulin receptor gene (INSR) locus, which is linked to LDLR, in relation to plasma lipids, body mass index and blood pressure in 27 obese and 57 non-obese Caucasians with severe essential hypertension, selected on the basis of having parents who were both hypertensive, and in 25 obese and 45 non-obese normotensive subjects selected on the basis of having parents who were both normotensive after the age of 50 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:7913431
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prov:wasDerivedFrom
dgn-void:befree-20140225
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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:NP300149.RA8rDZ8q63bwbcmVbSv53z4LTiWQUSP9peQbVDe1wdC4I130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
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prv:usedData
dgn-void:disgenetrdf
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> , <
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> , <
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> ;
pav:createdBy
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> ;
pav:version
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