@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM
> .
@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:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_head
{
this:
np:hasAssertion
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion
;
np:hasProvenance
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion
a
np:Assertion
.
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_provenance
a
np:Provenance
.
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGNec9737c6807d09825763fc1d3b6519b2
sio:SIO_000628
miriam-gene:7124
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_provenance
{
dgn-np:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_assertion
dcterms:description
"[Abstract A host of clinical scenarios can be depicted in hereditary autoinflammatory diseases, and the cardiovascular system can also be involved especially in familial Mediterranean fever (FMF), caused by mutations in the MEFV gene, and tumour necrosis factor receptor-associated periodic syndrome (TRAPS), caused by mutations in the TNFRSF1A gene.]. 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:21284530
;
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:NP550878.RAO3Vk5cmm-PBY8APIc0kp2KoYL9zIt_ZZ9WBAVh5aDMM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}