@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA
> .
@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:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_head
{
this:
np:hasAssertion
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion
;
np:hasProvenance
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_provenance
;
np:hasPublicationInfo
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion
a
np:Assertion
.
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_provenance
a
np:Provenance
.
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion
{
miriam-gene:2591
a
ncit:C16612
.
lld:C0085681
a
ncit:C7057
.
dgn-gda:DGN3476f157dea343cbb5f7f2fb87bce988
sio:SIO_000628
miriam-gene:2591
,
lld:C0085681
;
a
sio:SIO_001121
.
}
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_provenance
{
dgn-np:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_assertion
dcterms:description
"[The elucidation of the molecular basis of HFTC shed new light upon the mechanisms regulating phosphate homeostasis, suggesting innovative therapeutic strategies for the management of hyperphosphatemia in common acquired conditions such as chronic renal failure.]. 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:19013236
;
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:NP355752.RAavPA8fPM2c20OZTBjS7wcVd257h2YHzCus37xYOxTXA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:28+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" .
}