@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk
> .
@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:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_head
{
this:
np:hasAssertion
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_assertion
;
np:hasProvenance
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_provenance
;
np:hasPublicationInfo
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_assertion
a
np:Assertion
.
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_provenance
a
np:Provenance
.
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGN685ab40129cfcf2b5d15222b123e2a84
sio:SIO_000628
miriam-gene:4210
,
lld:C0002726
;
a
sio:SIO_001121
.
}
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_provenance
{
dgn-np:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_assertion
dcterms:description
"[We compared the frequencies of seven MEFV mutations (M694V, M680I, V726A, M694I, K695R, R761H, E148Q) and the clinical findings in 20 Turkish FMF patients who had not developed amyloidosis by the age of 40 years in the absence of colchicine therapy, with those in 27 Turkish amyloidosis patients.]. 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:11029479
;
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:NP252856.RAlTHWd2pnt03ta9sZ4XZxNuVsToj35X9SYBdG_d6gpMk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}