@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo
> .
@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:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_head
{
this:
np:hasAssertion
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_assertion
;
np:hasProvenance
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_provenance
;
np:hasPublicationInfo
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_assertion
a
np:Assertion
.
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_provenance
a
np:Provenance
.
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_assertion
{
miriam-gene:5745
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGNca63fca9e53dfd65ac57bb078335a4d8
sio:SIO_000628
miriam-gene:5745
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_provenance
{
dgn-np:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_assertion
dcterms:description
"[Based on the growth plate abnormalities observed in these human disorders and in mice with abnormal expression of either PTHrP or the PTH1R, it appears plausible that impaired expression of PTHrP and/or its receptor contributes to the growth abnormalities in children with end-stage renal disease.]. 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:10912527
;
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:NP544211.RA5YLF0OG47FqVJkbVHGaOjHwr-DNx5M7aFY0tltmgRRo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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" .
}