@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg
> .
@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:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_head
{
this:
np:hasAssertion
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_assertion
;
np:hasProvenance
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_assertion
a
np:Assertion
.
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_provenance
a
np:Provenance
.
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0085548
a
ncit:C7057
.
dgn-gda:DGNee760353d07de8c45b40810c8ef60a02
sio:SIO_000628
miriam-gene:1956
,
lld:C0085548
;
a
sio:SIO_001121
.
}
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_provenance
{
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_assertion
dcterms:description
"[A consistent phenotype observed in both human patients and several different mouse models of autosomal recessive polycystic kidney disease (ARPKD) is an increased activity of the epidermal growth factor receptor (EGFR) in the affected kidneys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:9486961
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP14583.RAvCmlKYr2gv6-xavy1N8UeKDpotxVsN9A04K3nTT6tEg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:05+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" .
}