@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc
> .
@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:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_head
{
this:
np:hasAssertion
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_assertion
;
np:hasProvenance
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_assertion
a
np:Assertion
.
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_provenance
a
np:Provenance
.
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0221014
a
ncit:C7057
.
dgn-gda:DGNe3456dfa5746228ce1046551796699c1
sio:SIO_000628
miriam-gene:4210
,
lld:C0221014
;
a
sio:SIO_001121
.
}
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_provenance
{
dgn-np:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_assertion
dcterms:description
"[Our identification of the pyrin Q148 allele in several patients from ethnic groups in which FMF is not classically recognized who had longstanding fevers or AA amyloidosis prompted us to study the prevalence of pyrin Q148 in healthy British, Indian and Chinese subjects.]. 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:11588211
;
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:NP177995.RA7rzgZ9oWd5fG40iXTGlpOqDeEK7RqhUQedrvShe_mAc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}