@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0
> .
@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:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_head
{
this:
np:hasAssertion
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_assertion
;
np:hasProvenance
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_provenance
;
np:hasPublicationInfo
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_assertion
a
np:Assertion
.
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_provenance
a
np:Provenance
.
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C1449647
a
ncit:C7057
.
dgn-gda:DGN1712dcda960bd0d6b73fa5efbfefb7be
sio:SIO_000628
miriam-gene:3953
,
lld:C1449647
;
a
sio:SIO_001121
.
}
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_provenance
{
dgn-np:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_assertion
dcterms:description
"[As gene variants of LEP and LEPR have been associated with diverse pathologic conditions, we explored the association of genetic polymorphisms of LEP or LEPR with death in patients with secondary peritonitis.]. 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:21943151
;
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:NP512151.RA_HVWKgDin6A_72aumxjCehE_r9P90y-ORF4E3Cs3kS0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}