@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ
> .
@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:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_head
{
this:
np:hasAssertion
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_assertion
;
np:hasProvenance
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_assertion
a
np:Assertion
.
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_provenance
a
np:Provenance
.
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0013336
a
ncit:C7057
.
dgn-gda:DGNc70e94e7a13f4cdb8d03709c843d6b38
sio:SIO_000628
miriam-gene:5741
,
lld:C0013336
;
a
sio:SIO_001121
.
}
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_provenance
{
dgn-np:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_assertion
dcterms:description
"[Pseudohypoparathyroidism type Ia (PHP-Ia) is a hereditary disorder characterized by resistance to multiple hormones that work via cAMP such as PTH and TSH, accompanied by typical skeletal features including short stature and brachydactyly, termed Albright hereditary osteodystrophy (AHO).]. 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:17803690
;
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:NP590036.RAz12DHbTrXNQNbQt9p6rPTWgKPABO3DqaHkfB2HXSCaQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}