@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8
> .
@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:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_head
{
this:
np:hasAssertion
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_assertion
;
np:hasProvenance
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_provenance
;
np:hasPublicationInfo
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_assertion
a
np:Assertion
.
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_provenance
a
np:Provenance
.
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C1274103
a
ncit:C7057
.
dgn-gda:DGN9ac62dd87c9f62747221b7b3059eec0c
sio:SIO_000628
miriam-gene:5741
,
lld:C1274103
;
a
sio:SIO_001121
.
}
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_provenance
{
dgn-np:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_assertion
dcterms:description
"[Oncogenic osteomalacia (OOM), X-linked hypophosphatemia (XLH), and autosomal dominant hypophosphatemic rickets (ADHR) are phenotypically similar disorders characterized by hypophosphatemia, decreased renal phosphate reabsorption, normal or low serum calcitriol concentrations, normal serum concentrations of calcium and parathyroid hormone, and defective skeletal mineralization.]. 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:11409890
;
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:NP601187.RAsRzLVE8LCgkrmv0VBHwh_M5THPgwdZigy_GcJj_WDc8130_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" .
}