@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8
> .
@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:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_head
{
this:
np:hasAssertion
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_assertion
;
np:hasProvenance
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_provenance
;
np:hasPublicationInfo
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_assertion
a
np:Assertion
.
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_provenance
a
np:Provenance
.
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_assertion
{
miriam-gene:728378
a
ncit:C16612
.
lld:C0268079
a
ncit:C7057
.
dgn-gda:DGN71c0c5e35c863cb70c1892213c7948be
sio:SIO_000628
miriam-gene:728378
,
lld:C0268079
;
a
sio:SIO_001121
.
}
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_provenance
{
dgn-np:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_assertion
dcterms:description
"[Overexpression of human PHEX under the human beta-actin promoter in Hyp mice rescued the bone phenotype almost completely, but did not affect phosphate homeostasis, suggesting that different, possibly independent, pathophysiological mechanisms contribute to hyperphosphaturia and bone abnormalities in XLH.]. 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:15940367
;
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:NP266972.RAwf7_R-gy1tBUBZ66FMC4gjyMEZI_uqbJky25V80r0x8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}