@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0
> .
@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:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_head
{
this:
np:hasAssertion
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_assertion
;
np:hasProvenance
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_provenance
;
np:hasPublicationInfo
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_assertion
a
np:Assertion
.
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_provenance
a
np:Provenance
.
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_assertion
{
miriam-gene:3934
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNd0d3cb378c1dce70654f69f56db104a9
sio:SIO_000628
miriam-gene:3934
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_provenance
{
dgn-np:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_assertion
dcterms:description
"[On the basis of data reported in the literature, it is reasonable to forecast an increasing clinical use of uNGAL capable to change our approach to the diagnosis and leading to better preventative and therapeutic interventions which will improve outcomes of critically ill infants with acute kidney disease.]. 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:20807163
;
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:NP617928.RAP5nayfCr_awSRkMV0CrlqLCD5HZQqqu0Vo4BPZBmxT0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}