@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI
> .
@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:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_head
{
this:
np:hasAssertion
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_assertion
;
np:hasProvenance
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_assertion
a
np:Assertion
.
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_provenance
a
np:Provenance
.
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_assertion
{
miriam-gene:3778
a
ncit:C16612
.
lld:C0343532
a
ncit:C7057
.
dgn-gda:DGN7e3848183088f9dc8c40d5b8d1c615be
sio:SIO_000628
miriam-gene:3778
,
lld:C0343532
;
a
sio:SIO_001121
.
}
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_provenance
{
dgn-np:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_assertion
dcterms:description
"[The rgg mutants from STSS clinical isolates enhanced lethality and impaired various organs in the mouse models, similar to the csrS mutants, and precluded their being killed by human neutrophils, mainly due to an overproduction of SLO.]. 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:20368967
;
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:NP494321.RA0DzuBoC69wVCs-Fki9qSNScOAu9zkpNpacpq8nV1bNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:55+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" .
}