@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs
> .
@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:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_head
{
this:
np:hasAssertion
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_assertion
;
np:hasProvenance
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_provenance
;
np:hasPublicationInfo
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_assertion
a
np:Assertion
.
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_provenance
a
np:Provenance
.
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_assertion
{
miriam-gene:5251
a
ncit:C16612
.
lld:C0035579
a
ncit:C7057
.
dgn-gda:DGN442515cf0533c23fe7c8626ec78e4834
sio:SIO_000628
miriam-gene:5251
,
lld:C0035579
;
a
sio:SIO_001121
.
}
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_provenance
{
dgn-np:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_assertion
dcterms:description
"[XLH is an important disease, it is the subject of several classic articles in the medical sciences (Scriver et al., 1991), and it has been an important stimulus to study renal hypophosphatemias and how they are involved in rickets and osteomalacia (Scriver, 1974; Scriver and Tenenhouse, 1991).]. 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:1592145
;
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:NP761828.RA9DoZ0MN7sQ5qQXEKPWRS2EMhwNoILFU4WuHiK7CkkCs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}