@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo
> .
@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:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_head
{
this:
np:hasAssertion
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_assertion
;
np:hasProvenance
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_provenance
;
np:hasPublicationInfo
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_assertion
a
np:Assertion
.
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_provenance
a
np:Provenance
.
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_assertion
{
miriam-gene:84224
a
ncit:C16612
.
lld:C0085548
a
ncit:C7057
.
dgn-gda:DGNaf546e75f51947d6031257bc41e376f2
sio:SIO_000628
miriam-gene:84224
,
lld:C0085548
;
a
sio:SIO_001121
.
}
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_provenance
{
dgn-np:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_assertion
dcterms:description
"[Our data suggest that hepatic cystogenesis in autosomal recessive polycystic kidney disease may involve increased fluid accumulation because of overexpression and abnormal location of AQP1, CFTR, and AE2 in cystic cholangiocytes.]. 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:18988797
;
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:NP456458.RAMEFGrlVghbv_JcF8-IKi2h-bC7IOyf_Mapaxg6qOUSo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}