@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24
> .
@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:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_head
{
this:
np:hasAssertion
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_assertion
;
np:hasProvenance
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_provenance
;
np:hasPublicationInfo
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_assertion
a
np:Assertion
.
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_provenance
a
np:Provenance
.
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C2931404
a
ncit:C7057
.
dgn-gda:DGNf1145841a224732e0be254da9ff82ca3
sio:SIO_000628
miriam-gene:5741
,
lld:C2931404
;
a
sio:SIO_001121
.
}
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_provenance
{
dgn-np:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_assertion
dcterms:description
"[Because patients with PHP type Ib do not have Albright's hereditary osteodystrophy, and because resistance to PTH is most prominent in proximal tubules of the kidney, PHP Ib may be caused by a kidney-specific abnormality in PTH/PTHrP receptor.]. 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:9723884
;
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:NP344840.RAuQi6bFpZS4G36DNijq8mMHcQd-tJfVsMUI8d7BVNk24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}