@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI
> .
@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:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_head
{
this:
np:hasAssertion
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_assertion
;
np:hasProvenance
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_provenance
;
np:hasPublicationInfo
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_assertion
a
np:Assertion
.
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_provenance
a
np:Provenance
.
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_assertion
{
miriam-gene:649
a
ncit:C16612
.
lld:C0032305
a
ncit:C7057
.
dgn-gda:DGN64c000d7eefccf07af152a2c4002e868
sio:SIO_000628
miriam-gene:649
,
lld:C0032305
;
a
sio:SIO_001121
.
}
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_provenance
{
dgn-np:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_assertion
dcterms:description
"[Exciting data implicate PCP in normal kidney development and suggest the loss of oriented cell division and convergent extension downstream of defective PCP signaling lead to cystic kidney disease in mouse models.]. 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:19762494
;
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:NP600974.RA0LmlOlo1MXciM2vmuHo_PLGQJEfJN3-oIe3IS6W1uQI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}