@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg
> .
@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:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_head
{
this:
np:hasAssertion
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion
;
np:hasProvenance
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion
a
np:Assertion
.
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_provenance
a
np:Provenance
.
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion
{
miriam-gene:6285
a
ncit:C16612
.
lld:C0022116
a
ncit:C7057
.
dgn-gda:DGNc3dd7a58bfdd894c2278ba807f7bf081
sio:SIO_000628
miriam-gene:6285
,
lld:C0022116
;
a
sio:SIO_001121
.
}
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_provenance
{
dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion
dcterms:description
"[Hence, S100B, far from being a negative determinant of outcome, as suggested previously in the human TBI and ischemia literature, is of potential therapeutic value that could improve outcome in patients who sustain various forms of acute brain damage.]. 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:16928177
;
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:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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
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"v2.1.0" .
}