@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw
> .
@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:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_head
{
this:
np:hasAssertion
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_assertion
;
np:hasProvenance
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_provenance
;
np:hasPublicationInfo
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_assertion
a
np:Assertion
.
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_provenance
a
np:Provenance
.
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_assertion
{
miriam-gene:55278
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN1ae72f9d9c82916ccd68ec6e90ca5f90
sio:SIO_000628
miriam-gene:55278
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_provenance
{
dgn-np:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_assertion
dcterms:description
"[These results show that GATA3 is essential in the embryonic development of the parathyroids, auditory system and kidneys, and indicate that other GATA family members may be involved in the aetiology of human malformations.]. 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:10935639
;
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:NP677845.RANeliImp5HfZmGUQffzFWEWohHlm9oEHJCY7TEFIwOaw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}