@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_assertion
;
np:hasProvenance
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_provenance
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np:hasPublicationInfo
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_assertion
a
np:Assertion
.
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_provenance
a
np:Provenance
.
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_assertion
{
miriam-gene:3312
a
ncit:C16612
.
lld:C0022660
a
ncit:C7057
.
dgn-gda:DGNe02e39bff7da7a78d0d25bb591e3a19d
sio:SIO_000628
miriam-gene:3312
,
lld:C0022660
;
a
sio:SIO_001121
.
}
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_provenance
{
dgn-np:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_assertion
dcterms:description
"[We have investigated the association of genetic polymorphisms of the constitutive HSP70 (HSP73) and the inducible HSP70 (HSP72) encoding genes with the risk of acute renal failure (ARF) in very low birth weight (VLBW) neonates.]. 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:12840151
;
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:NP159235.RAVOkIUnsgodXsZkDQvIFV1XkoDq2CUl4PquFy3BvJM6I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}