@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko
> .
@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:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_head
{
this:
np:hasAssertion
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion
;
np:hasProvenance
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_provenance
;
np:hasPublicationInfo
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion
a
np:Assertion
.
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_provenance
a
np:Provenance
.
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion
{
miriam-gene:4210
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN9f778c6368abe20bdc83684ab5db4bee
sio:SIO_000628
miriam-gene:4210
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_provenance
{
dgn-np:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_assertion
dcterms:description
"[MEFV mutation carriage appears to modify the SLE disease phenotype in that it contributes to an excess of inflammatory manifestations such as fever and pleuritis on the one hand, while thwarting more severe renal involvement on the other.]. 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:22532615
;
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:NP643333.RAc3g7TbGognmb91Latk0Ba7jGDXuvWfLWxeaR4PI_0Ko130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:27+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" .
}