@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM
> .
@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:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_head
{
this:
np:hasAssertion
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion
;
np:hasProvenance
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion
a
np:Assertion
.
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_provenance
a
np:Provenance
.
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0035436
a
ncit:C7057
.
dgn-gda:DGNfef31294af0ebcd2b5a15cafd2f69538
sio:SIO_000628
miriam-gene:4153
,
lld:C0035436
;
a
sio:SIO_001121
.
}
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_provenance
{
dgn-np:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_assertion
dcterms:description
"[As high levels of MBL and MBL2 associated genotypes have previously been seen to be associated with CRHD, we investigated the association between MBL2 polymorphisms and the presence of acute carditis and arthritis in patients with a history of RF.]. 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:18602696
;
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:NP500436.RAEmjXOxP1fl9vwzBa0T5TG6q5JII3jjQcMkon5T2vsQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}