@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_head
{
this:
np:hasAssertion
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_assertion
a
np:Assertion
.
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_provenance
a
np:Provenance
.
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0268382
a
ncit:C7057
.
dgn-gda:DGN092e9808527f8eef7045dae4e22ec654
sio:SIO_000628
miriam-gene:4210
,
lld:C0268382
;
a
sio:SIO_001121
.
}
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_provenance
{
dgn-np:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_assertion
dcterms:description
"[Molecular analysis of MEFV gene mutations in 3000 Armenian patients has demonstrated direct correlation between the clinical severity and the molecular diagnostic criteria of the disease, including the development of renal amyloidosis with MEFV genotypes.]. 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:15720244
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP481536.RAovlnOyhda-BQ6OC42TjSEWFeXSmzoNzEyrIdgJyZjz4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:23+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}