@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY
> .
@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:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_head
{
this:
np:hasAssertion
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_assertion
;
np:hasProvenance
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_assertion
a
np:Assertion
.
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_provenance
a
np:Provenance
.
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_assertion
{
miriam-gene:79447
a
ncit:C16612
.
lld:C0037278
a
ncit:C7057
.
dgn-gda:DGNc774d7b364d6d607ec57d97ff9553abc
sio:SIO_000628
miriam-gene:79447
,
lld:C0037278
;
a
sio:SIO_001121
.
}
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_provenance
{
dgn-np:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_assertion
dcterms:description
"[Deletion of sse(M28) in a covS deletion mutant of GAS increased neutrophil recruitment and reduced skin infection, whereas in trans expression of SsE(M28) in GAS reduced neutrophil infiltration and increased skin invasion in subcutaneous infection of mice.]. 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:23774595
;
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:NP930037.RAUZYtz8DXYUAmFWE9fZJ4cVff894cjdZIxjNerAMUeFY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:30+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" .
}