@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg
> .
@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:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_head
{
this:
np:hasAssertion
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_assertion
;
np:hasProvenance
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_provenance
;
np:hasPublicationInfo
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_assertion
a
np:Assertion
.
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_provenance
a
np:Provenance
.
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_assertion
{
miriam-gene:6288
a
ncit:C16612
.
lld:C0221014
a
ncit:C7057
.
dgn-gda:DGN6d9f3e4e6627e71edb65ede98225a447
sio:SIO_000628
miriam-gene:6288
,
lld:C0221014
;
a
sio:SIO_001121
.
}
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_provenance
{
dgn-np:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_assertion
dcterms:description
"[These findings suggest that -13T is a genetic background for AA amyloidosis in both Japanese and Caucasians and the difference in prevalence of AA amyloidosis in the two ethnic groups may be due, at least in part, to a difference in the frequency of the -13T SAA1 allele.]. 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:12762135
;
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:NP277314.RAteFHL8xnUFyUdlebk0iYXObEO3IagHPMhBdDYnAZcTg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}