@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc
> .
@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:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_head
{
this:
np:hasAssertion
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_assertion
;
np:hasProvenance
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_provenance
;
np:hasPublicationInfo
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_assertion
a
np:Assertion
.
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_provenance
a
np:Provenance
.
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNae73452adb3bb7e52ce0ffe7a3116175
sio:SIO_000628
miriam-gene:3953
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_provenance
{
dgn-np:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_assertion
dcterms:description
"[When BMI and leptin are elevated, increased blood pressure is found only with the most prevalent LEPR genotype at codons 109 and 223, whereas variants of this receptor seem to protect from hypertension.]. 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:10999797
;
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:NP715966.RAC3UJV8s_cBi2S1yBMcVRBd5FnSw_aIEYajGIPJn9Kfc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}