@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA
> .
@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:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_head
{
this:
np:hasAssertion
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_assertion
;
np:hasProvenance
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_assertion
a
np:Assertion
.
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_provenance
a
np:Provenance
.
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_assertion
{
miriam-gene:4069
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGN6a762fc57316d791f47d1b4bf17e3e50
sio:SIO_000628
miriam-gene:4069
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_provenance
{
dgn-np:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_assertion
dcterms:description
"[Molecular genetic testing of the MEFV gene, the only gene currently known to be associated with familial Mediterranean fever, can be offered to family members, especially when the p.Met694Val allele is present, because renal amyloidosis can be prevented by colchicine.]. 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:21358337
;
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:NP506939.RAiwvCGgF-_T8UkC_V5HEZs_e2cTDB9dfQk8AVkF2wPOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}