@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs
> .
@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:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_head
{
this:
np:hasAssertion
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_assertion
;
np:hasProvenance
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_provenance
;
np:hasPublicationInfo
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_assertion
a
np:Assertion
.
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_provenance
a
np:Provenance
.
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_assertion
{
miriam-gene:1482
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGN038765685f121dae7157cdcec7048e47
sio:SIO_000628
miriam-gene:1482
,
lld:C0152021
;
a
sio:SIO_001121
.
}
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_provenance
{
dgn-np:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_assertion
dcterms:description
"[The frequency of GATA4, NKX2.5, and TFAP2B mutations in subjects with congenital heart disease in southern China and the correlation between their genotype and congenital heart disease phenotype are not known.]. 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:22959235
;
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:NP167042.RAXyInj5tvBNDUBFPWmovPh6wkL-vsZnIU6bYhLqeOPSs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}