@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc
> .
@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:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_head
{
this:
np:hasAssertion
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_assertion
;
np:hasProvenance
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_provenance
;
np:hasPublicationInfo
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_assertion
a
np:Assertion
.
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_provenance
a
np:Provenance
.
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_assertion
{
miriam-gene:3859
a
ncit:C16612
.
lld:C0009319
a
ncit:C7057
.
dgn-gda:DGNc149f98a045840724693e0c299b3e244
sio:SIO_000628
miriam-gene:3859
,
lld:C0009319
;
a
sio:SIO_001121
.
}
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_provenance
{
dgn-np:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_assertion
dcterms:description
"[Moreover, in the LF82 strain, the replacement of fimH(LF82) (expressing FimH with an AIEC-associated mutation) with fimH(K12) (expressing FimH of commensal E. coli K12) decreased the ability of bacteria to persist and to induce severe colitis and gut inflammation in infected CEABAC10 transgenic mice expressing human CEACAM receptors.]. 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:23358328
;
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:NP702140.RAE4VTLTt_3IEHMV3V7mVIRWV5XqO8Q_26IB-Um3PW5Lc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:07+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" .
}