@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_head
{
this:
np:hasAssertion
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_assertion
a
np:Assertion
.
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_provenance
a
np:Provenance
.
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:5741
a
ncit:C16612
.
lld:C3494506
a
ncit:C7057
.
dgn-gda:DGN35ecec5358c994d048fe923c3a10c195
sio:SIO_000628
miriam-gene:5741
,
lld:C3494506
;
a
sio:SIO_001121
.
}
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_provenance
{
dgn-np:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_assertion
dcterms:description
"[While loss-of-function mutations in Gsalpha are invariably associated with the short stature and brachydactyly of Albright hereditary osteodystrophy (AHO), the association with hormone resistance (to parathyroid hormone and thyrotropin) typical of pseudohypoparathyroidism type Ia (PHP-Ia) is much more variable.]. 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:9600732
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1395887.RAuwapwX-Nr-wGhSfe7cyZEpmmEouoLq7XRrpBov4eCNM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:19+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
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;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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
"v4.0.0.0" .
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"v4.0.0" .
}