@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg
> .
@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:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_head
{
this:
np:hasAssertion
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_assertion
;
np:hasProvenance
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_assertion
a
np:Assertion
.
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_provenance
a
np:Provenance
.
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_assertion
{
miriam-gene:7124
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGNc0ce9f65ab6264d4cd575080d09ae059
sio:SIO_000628
miriam-gene:7124
,
lld:C0002726
;
a
sio:SIO_001121
.
}
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_provenance
{
dgn-np:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_assertion
dcterms:description
"[This study shows that circulating levels of TNFalpha and sTNFRI are significantly increased in RA patients with amyloidosis as compared with control RA patients without amyloidosis and that the increased levels may be implicated in the pathogenesis of certain disease manifestations, including anemia of chronic disease and renal pathology in reactive amyloidosis.]. 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:14613268
;
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:NP405160.RA0z8YH29GarsSvXJPT2F3VEO4TGHvUrY5kmHiTCc4Pfg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}