@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU
> .
@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:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_head
{
this:
np:hasAssertion
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion
;
np:hasProvenance
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_provenance
;
np:hasPublicationInfo
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion
a
np:Assertion
.
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_provenance
a
np:Provenance
.
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion
{
miriam-gene:55349
a
ncit:C16612
.
lld:C0018818
a
ncit:C7057
.
dgn-gda:DGNe47cd2190eac20d3617fbd8fee615dc1
sio:SIO_000628
miriam-gene:55349
,
lld:C0018818
;
a
sio:SIO_001121
.
}
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_provenance
{
dgn-np:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_assertion
dcterms:description
"[The goal of our study was to identify potential pathogenic mutations in the TDGF1 gene in Chinese people with isolated CHD, particularly those with VSD, and to provide further insight into the etiology of CHD.]. 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:19853938
;
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:NP178315.RAm4l8YtPjI_eqj5BrMs7xEDtglgU3EEjbLQxoiZudaEU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}