@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA
> .
@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:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_head
{
this:
np:hasAssertion
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_assertion
;
np:hasProvenance
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_assertion
a
np:Assertion
.
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_provenance
a
np:Provenance
.
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN369134e3c307b3cf86493c25bc408f8f
sio:SIO_000628
miriam-gene:4210
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_provenance
{
dgn-np:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_assertion
dcterms:description
"[Familial Mediterranean Fever (FMF) is an autosomal, recessively inherited disease, characterized by recurrent and short attacks of fever with serosal inflammation that are caused by mutations in MEFV gene that encodes pyrin protein.]. 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:18177465
;
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:NP870598.RAVaecA0GzMTmynEFJ4HEI4DIdKECWjHkn4wa_NQCIcyA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}