@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0
> .
@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:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_head
{
this:
np:hasAssertion
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_assertion
;
np:hasProvenance
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_provenance
;
np:hasPublicationInfo
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_assertion
a
np:Assertion
.
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_provenance
a
np:Provenance
.
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C2932716
a
ncit:C7057
.
dgn-gda:DGNef0b64ec974ba9192750a1cebc0b178c
sio:SIO_000628
miriam-gene:2778
,
lld:C2932716
;
a
sio:SIO_001121
.
}
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_provenance
{
dgn-np:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_assertion
dcterms:description
"[We conducted clinical and biological studies including screening for mutations in the gene encoding the alpha subunit of G(s) (GNAS1) in 30 subjects (21 unrelated families) with Albright's hereditary osteodystrophy (AHO), pseudohypoparathyroidism (PHP); and decreased erythrocyte G(s) activity (PHP-Ia; n = 19); AHO and decreased erythrocyte G(s) activity (isolated AHO; n = 10); or AHO, hormonal resistance, and normal erythrocyte G(s) activity (PHP-Ic; n = 1).]. 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:11788646
;
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:NP274114.RAIv2OZvS7xHMQCfWIWqsJPVI7zv7TPoE0yn86rbSHDC0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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
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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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}