@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y
> .
@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:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_head
{
this:
np:hasAssertion
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_assertion
;
np:hasProvenance
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_assertion
a
np:Assertion
.
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_provenance
a
np:Provenance
.
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0221357
a
ncit:C7057
.
dgn-gda:DGNfb63b885c76b86a04444806679193c29
sio:SIO_000628
miriam-gene:5741
,
lld:C0221357
;
a
sio:SIO_001121
.
}
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_provenance
{
dgn-np:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_assertion
dcterms:description
"[Albright's hereditary osteodystrophy (AHO) is characterized by phenotypic signs that typically include brachydactyly and sc calcifications occurring with or without hormone resistance toward PTH or other hormones such as thyroid hormone or gonadotropins.]. 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:11600516
;
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:NP333169.RA_mA0ogW9pinlwmXd0ALdKqosddbWLxR6cvFQJY06O3Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}