@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU
> .
@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:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_head
{
this:
np:hasAssertion
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_assertion
;
np:hasProvenance
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_provenance
;
np:hasPublicationInfo
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_assertion
a
np:Assertion
.
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_provenance
a
np:Provenance
.
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_assertion
{
miriam-gene:4358
a
ncit:C16612
.
lld:C0392525
a
ncit:C7057
.
dgn-gda:DGNf0d6e5a7e0f451f3efaf03686b7ab250
sio:SIO_000628
miriam-gene:4358
,
lld:C0392525
;
a
sio:SIO_001121
.
}
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_provenance
{
dgn-np:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_assertion
dcterms:description
"[Renal tubular dysfunction may be evident even in the neonatal period, hypophosphatemic rickets may develop in the first years of life, and nephrocalcinosis (but not nephrolithiasis) with glomerulosclerosis are consistent features in childhood.]. 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:9811383
;
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:NP412619.RAsC1qkm7nq8MoBrcfrz4bP0WJ40Qu2kImHQEjkbir3PU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}