@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI
> .
@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:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_head
{
this:
np:hasAssertion
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_assertion
;
np:hasProvenance
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_provenance
;
np:hasPublicationInfo
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_assertion
a
np:Assertion
.
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_provenance
a
np:Provenance
.
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_assertion
{
miriam-gene:4069
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGN6270b420cba3d13085c7eea8aa6f3c25
sio:SIO_000628
miriam-gene:4069
,
lld:C0002726
;
a
sio:SIO_001121
.
}
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_provenance
{
dgn-np:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_assertion
dcterms:description
"[The aim of this study was to examine the controversial issue of amyloidosis susceptibility in FMF by determining the relative contributions of MEFV and numerous epidemiologic factors to the risk of renal amyloidosis.]. 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:17469185
;
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:NP465452.RA82FgZ1y4m0Gwd6zHZx9lJZaTftl26Wnhwl-HISKHdAI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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" .
}