@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k
> .
@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:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_head
{
this:
np:hasAssertion
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_assertion
;
np:hasProvenance
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_provenance
;
np:hasPublicationInfo
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_assertion
a
np:Assertion
.
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_provenance
a
np:Provenance
.
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_assertion
{
miriam-gene:57057
a
ncit:C16612
.
lld:C0018817
a
ncit:C7057
.
dgn-gda:DGN11f6260a00d8918e0d5685849013f3e5
sio:SIO_000628
miriam-gene:57057
,
lld:C0018817
;
a
sio:SIO_001121
.
}
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_provenance
{
dgn-np:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_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
;
sio:SIO_000772
miriam-pubmed:18834961
;
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:NP766611.RAb6SLlN29mf3B9VTEu84wo_NrjzVOaAlzAw6-VXKNN2k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}