@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4
> .
@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:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_head
{
this:
np:hasAssertion
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_assertion
;
np:hasProvenance
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_provenance
;
np:hasPublicationInfo
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_assertion
a
np:Assertion
.
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_provenance
a
np:Provenance
.
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_assertion
{
miriam-gene:5314
a
ncit:C16612
.
lld:C0010709
a
ncit:C7057
.
dgn-gda:DGNcb782caf3fa30f90e33912e2b8af45a9
sio:SIO_000628
miriam-gene:5314
,
lld:C0010709
;
a
sio:SIO_001122
.
}
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_provenance
{
dgn-np:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_assertion
dcterms:description
"[These results suggest that the loss of fibrocystin may lead to abnormal proliferation in kidney epithelial cells and cyst formation in autosomal recessive polycystic kidney disease by modulation of intracellular Ca (2+).]. 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:17669261
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP132696.RA3A56pyNB2Di88zypS6EMu1Zla8OiMdrYFyrhhpVVhK4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:09+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" .
}