@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE
> .
@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:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_head
{
this:
np:hasAssertion
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_assertion
;
np:hasProvenance
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_provenance
;
np:hasPublicationInfo
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_assertion
a
np:Assertion
.
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_provenance
a
np:Provenance
.
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_assertion
{
miriam-gene:7132
a
ncit:C16612
.
lld:C1275126
a
ncit:C7057
.
dgn-gda:DGN54d842afbd4f4654368556d5440d89d6
sio:SIO_000628
miriam-gene:7132
,
lld:C1275126
;
a
sio:SIO_001122
.
}
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_provenance
{
dgn-np:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_assertion
dcterms:description
"[The frequency of typical TRAPS-related clinical manifestations was significantly lower and the impact of the disease on HRQOL was significantly reduced in patients with the R92Q mutation compared with TRAPS patients carrying structural mutations of TNFRSF1A.]. 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:21225694
;
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:NP864773.RAYRN9ZlNYZx6vg0BjDcUM8pRuY4NYBuUdbGsQM8vBccE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:16+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" .
}