@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw
> .
@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:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_head
{
this:
np:hasAssertion
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion
;
np:hasProvenance
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_provenance
;
np:hasPublicationInfo
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion
a
np:Assertion
.
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_provenance
a
np:Provenance
.
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion
{
miriam-gene:138428
a
ncit:C16612
.
lld:C0221357
a
ncit:C7057
.
dgn-gda:DGNa2f2265f5affa5db0b86da8b8fb57a16
sio:SIO_000628
miriam-gene:138428
,
lld:C0221357
;
a
sio:SIO_001121
.
}
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_provenance
{
dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_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-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:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}