@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4
> .
@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:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_head
{
this:
np:hasAssertion
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_assertion
;
np:hasProvenance
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_provenance
;
np:hasPublicationInfo
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_assertion
a
np:Assertion
.
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_provenance
a
np:Provenance
.
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_assertion
{
miriam-gene:50818
a
ncit:C16612
.
lld:C0085548
a
ncit:C7057
.
dgn-gda:DGN9d50229e2255d3722c8fceae27ee7dd9
sio:SIO_000628
miriam-gene:50818
,
lld:C0085548
;
a
sio:SIO_001121
.
}
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_provenance
{
dgn-np:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_assertion
dcterms:description
"[They demonstrate that levels of the miRNA miR15a are decreased in livers of patients with autosomal recessive and autosomal dominant polycystic kidney disease (ARPKD and ADPKD, respectively) and congenital hepatic fibrosis as well as in the PKC rat model of ARPKD.]. 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:18949060
;
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:NP697501.RA8WipMHGDHQ1Z6-fEn9rwYdOwq829kPwGlwAGRz1nus4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}