@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs
> .
@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:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_head
{
this:
np:hasAssertion
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_assertion
;
np:hasProvenance
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_assertion
a
np:Assertion
.
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_provenance
a
np:Provenance
.
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGNccac1177b0abec313e899661438128e3
sio:SIO_000628
miriam-gene:4210
,
lld:C0002726
;
a
sio:SIO_001122
.
}
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_provenance
{
dgn-np:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_assertion
dcterms:description
"[In phenotype II amyloidosis patients, the distribution of the four common MEFV mutations was not significantly different from that found in all FMF patients with typical symptoms who do or do not develop amyloidosis.]. 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:12401847
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP145223.RAuKBG_OxdxcrguoDDXmC3xTyvtrZ5A3StkkhWc2u9FYs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:16+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" .
}