@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo
> .
@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:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_head
{
this:
np:hasAssertion
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_assertion
;
np:hasProvenance
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_provenance
;
np:hasPublicationInfo
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_assertion
a
np:Assertion
.
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_provenance
a
np:Provenance
.
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_assertion
{
miriam-gene:7132
a
ncit:C16612
.
lld:C0231528
a
ncit:C7057
.
dgn-gda:DGN2aba15e2d4dbc7af35ea943c5d850161
sio:SIO_000628
miriam-gene:7132
,
lld:C0231528
;
a
sio:SIO_001121
.
}
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_provenance
{
dgn-np:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_assertion
dcterms:description
"[Among them it is recognized the TNF receptor associated periodic syndrome (TRAPS) caused by mutations in the TNFRSF1A gene and characterized by symptoms such as recurrent high fevers, rash, abdominal pain, arthralgia and myalgia.]. 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:21567205
;
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:NP748087.RA7ZFQbqPyh2jhEeuYbej3KHeDzGDKYlZS8uWSoZIafKo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}