@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w
> .
@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:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_head
{
this:
np:hasAssertion
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_assertion
;
np:hasProvenance
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_provenance
;
np:hasPublicationInfo
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_assertion
a
np:Assertion
.
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_provenance
a
np:Provenance
.
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGN255f77cbe1dae3574c8faa4633728993
sio:SIO_000628
miriam-gene:7124
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_provenance
{
dgn-np:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_assertion
dcterms:description
"[Among hereditary fevers characterized by recurrent attacks of fever and organ localized inflammation, familial Mediterranean fever (FMF), and tumour necrosis factor receptor superfamily 1A (TNFRSF1A) receptor associated periodic syndrome (TRAPS) are diseases with identified genes that can be associated with renal amyloidosis of the AA type.]. 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:12105243
;
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:NP606847.RA7_AqqiADLEp_VBWfJBhpDxNCq0nBcI9Zfvek2gLaz-w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}