@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8
> .
@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
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_assertion
a
np:Assertion
.
dgn-np:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_provenance
a
np:Provenance
.
dgn-np:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:3308
a
ncit:C16612
.
lld:C0022660
a
ncit:C7057
.
dgn-gda:DGN13cdfa044c43423fd69d513d86513a2a
sio:SIO_000628
miriam-gene:3308
,
lld:C0022660
;
a
sio:SIO_001121
.
}
dgn-np:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_provenance
{
dgn-np:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_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:NP447381.RAPDjjMmnXxxNGV1b4QDkE79AcorD4B9ngXA4a66D3jg8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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
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