@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_head
{
this:
np:hasAssertion
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_assertion
;
np:hasProvenance
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_assertion
a
np:Assertion
.
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_provenance
a
np:Provenance
.
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGNa62b2e5b9dc6310dc55025c0e7f87f76
sio:SIO_000628
miriam-gene:4210
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_provenance
{
dgn-np:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_assertion
dcterms:description
"[Pyrin Q148 is a polymorphism and occurs widely in global terms, and, although it may cause FMF when associated with certain other MEFV mutations, homozygosity for Q148 alone must usually be insufficient to produce FMF in the populations studied.]. 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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP332137.RAwuMqsBYMFbvaEuFTGHssh-GWGzqb7jWYwvaPiD_9fVQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}