@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE
> .
@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:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_head
{
this:
np:hasAssertion
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_assertion
;
np:hasProvenance
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_provenance
;
np:hasPublicationInfo
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_assertion
a
np:Assertion
.
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_provenance
a
np:Provenance
.
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_assertion
{
miriam-gene:2625
a
ncit:C16612
.
lld:C1840333
a
ncit:C7057
.
dgn-gda:DGN2d7f2611533d2532d2c55da2da719957
sio:SIO_000628
miriam-gene:2625
,
lld:C1840333
;
a
sio:SIO_001121
.
}
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_provenance
{
dgn-np:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_assertion
dcterms:description
"[No mutations were identified in patients with isolated hypoparathyroidism, thereby indicating that GATA3 abnormalities are more likely to result in two or more of the phenotypic features of the HDR syndrome and not in one, such as isolated hypoparathyroidism.]. 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:17210674
;
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:NP587720.RAxrnPGpZd2JIpMHf-MysekPOXJFPuM9w_3gORUBBvhjE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:11+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" .
}