@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o
> .
@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:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_head
{
this:
np:hasAssertion
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_assertion
;
np:hasProvenance
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_assertion
a
np:Assertion
.
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_provenance
a
np:Provenance
.
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0850497
a
ncit:C7057
.
dgn-gda:DGN7c603eaf41b8ff183cc78915f1fd780b
sio:SIO_000628
miriam-gene:5741
,
lld:C0850497
;
a
sio:SIO_001121
.
}
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_provenance
{
dgn-np:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_assertion
dcterms:description
"[We hypothesized that the stimulated (secretory reserve) but not the constitutive secretion of parathyroid hormone would be reduced in normocalcemic children with conotruncal cardiac defects but no overt immune deficiency and would be related to the presence of a deletion in the DiGeorge chromosomal region of 22q11.]. 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:8653876
;
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:NP914542.RA0EuneCF-bdBUTpCtazxmAyoMXARkZon7h8pJTZQzg1o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:21+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" .
}