@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk
> .
@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:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_head
{
this:
np:hasAssertion
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion
;
np:hasProvenance
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion
a
np:Assertion
.
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_provenance
a
np:Provenance
.
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGNa869e09fe552a90c52a17b2dc67ad274
sio:SIO_000628
miriam-gene:3953
,
lld:C0018801
;
a
sio:SIO_001122
.
}
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_provenance
{
dgn-np:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_assertion
dcterms:description
"[The aim of this study was to investigate the possible associations of defined variability in leptin (dbSNP ID rs7799039), proopiomelanocortin (dbSNP ID rs3754860 and dbSNP ID rs1009388), and leptin receptor gene (dbSNP rs1137101) with CHF and evaluate their potential as the CHF susceptibility genes.]. 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:19337797
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP70529.RAChwcQphpOBs1mlSRBxThr7YKDj_NbvWQF2mN5GfrPyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}