@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4
> .
@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:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_head
{
this:
np:hasAssertion
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_assertion
;
np:hasProvenance
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_assertion
a
np:Assertion
.
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_provenance
a
np:Provenance
.
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_assertion
{
miriam-gene:4267
a
ncit:C16612
.
lld:C2732473
a
ncit:C7057
.
dgn-gda:DGN6d93aa3b11dd66bf021f02851b57f60a
sio:SIO_000628
miriam-gene:4267
,
lld:C2732473
;
a
sio:SIO_001121
.
}
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_provenance
{
dgn-np:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_assertion
dcterms:description
"[Nearly all of those with a MIC in excess of European Committee on Antimicrobial Susceptibility Testing (EUCAST) resistance breakpoints contained one or more representatives of only seven gene types capable of explaining this phenotype, and this included 96% of those with a MIC ≥ 2 μg/mL to any one of these drugs.]. 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:23706544
;
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:NP614744.RAs3cF8F0497pKIeTT8Yx_zTGtTzz1vbk5rs-d5B2IVQ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}