@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8
> .
@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:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_head
{
this:
np:hasAssertion
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion
;
np:hasProvenance
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_provenance
;
np:hasPublicationInfo
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion
a
np:Assertion
.
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_provenance
a
np:Provenance
.
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion
{
miriam-gene:80347
a
ncit:C16612
.
lld:C3494506
a
ncit:C7057
.
dgn-gda:DGN033d71087bb5fe28815d4b05aad5f649
sio:SIO_000628
miriam-gene:80347
,
lld:C3494506
;
a
sio:SIO_001121
.
}
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_provenance
{
dgn-np:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_assertion
dcterms:description
"[Classically, patients with PHP have the skeletal features of AHO, resistance to multiple hormones that work via cAMP such as parathyroid hormone and thyroid stimulating hormone, and deficient activity of Gs protein, the guanine nucleotide-binding protein that stimulates adenylate cyclase.]. 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:1621772
;
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:NP186359.RAfgOgzGaUIs5mgorlX0WLkIx6p_gN8jXiQRhVZa2V2n8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}