@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs
> .
@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:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_head
{
this:
np:hasAssertion
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion
;
np:hasProvenance
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion
a
np:Assertion
.
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_provenance
a
np:Provenance
.
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion
{
miriam-gene:9495
a
ncit:C16612
.
lld:C0019061
a
ncit:C7057
.
dgn-gda:DGN8e1bccdfc2801f6edd598a8fe4fc9872
sio:SIO_000628
miriam-gene:9495
,
lld:C0019061
;
a
sio:SIO_001121
.
}
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_provenance
{
dgn-np:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_assertion
dcterms:description
"[In conclusion, potentially pathogenic O113:H21 STEC isolates carrying virulence markers in common with O113:H21 clones associated with haemolytic uraemic syndrome cases in other regions were demonstrated to occur in the natural reservoir in our settings, and therefore the risk represented by them to public health should be carefully monitored.]. 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:20223897
;
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:NP483079.RAt9qErLqiuLRG7p8k7Gt1erGptQQJ6eAkXN4mp3RpRIs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}