@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM
> .
@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:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_head
{
this:
np:hasAssertion
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_assertion
;
np:hasProvenance
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_provenance
;
np:hasPublicationInfo
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_assertion
a
np:Assertion
.
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_provenance
a
np:Provenance
.
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_assertion
{
miriam-gene:25870
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8649be9a276b5505bb43c97cea6be126
sio:SIO_000628
miriam-gene:25870
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_provenance
{
dgn-np:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_assertion
dcterms:description
"[Sixty vancomycin-resistant vanA mutant Enterococcus faecium (VRE) isolates, collected during a 40-month period from 48 patients hospitalized in a French Cancer Referral Center, were typed by using random amplified polymorphic DNA (RAPD), and the results were compared with those previously obtained by typing with SmaI pulsed-field gel electrophoresis (PFGE), which is currently recognized as the `gold standard.` The discriminating power of RAPD typing, with seven primers and 11 combinations of primers, was tested on 18 strains, and only the most discriminating combination was further tested on the whole collection.]. 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:8727883
;
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:NP885012.RASGHVV9LYnKnpd9U1MUtk4heHKwdUGdLoAr66vR0FwTM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}