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http://rdf.disgenet.org/nanopublications.trig#NP536145.RAXIDHCFlARF6ii65fjsdBxjMpw5Qp1NPpwf1zceqjTrY
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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;
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a
np:Nanopublication
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dgn-np:NP536145.RAXIDHCFlARF6ii65fjsdBxjMpw5Qp1NPpwf1zceqjTrY130_assertion
a
np:Assertion
.
dgn-np:NP536145.RAXIDHCFlARF6ii65fjsdBxjMpw5Qp1NPpwf1zceqjTrY130_provenance
a
np:Provenance
.
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{
miriam-gene:57057
a
ncit:C16612
.
lld:C0039685
a
ncit:C7057
.
dgn-gda:DGN9901b3f630a8debc057ed90f2530ed37
sio:SIO_000628
miriam-gene:57057
,
lld:C0039685
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.
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dgn-np:NP536145.RAXIDHCFlARF6ii65fjsdBxjMpw5Qp1NPpwf1zceqjTrY130_provenance
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dgn-np:NP536145.RAXIDHCFlARF6ii65fjsdBxjMpw5Qp1NPpwf1zceqjTrY130_assertion
dcterms:description
"[These data indicate that the frequency of TBX20 missense mutations occurred in Chinese CHD children is low, but they probably contribute to the risk of atrial septal defect (ASD), total anomalous pulmonary venous connection (TAPVC) and tetralogy of Fallot (TOF) in a small subset of Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:18834961
;
prov:wasDerivedFrom
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;
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
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dgn-np:NP536145.RAXIDHCFlARF6ii65fjsdBxjMpw5Qp1NPpwf1zceqjTrY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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