@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg
> .
@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:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_head
{
this:
np:hasAssertion
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_assertion
;
np:hasProvenance
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_assertion
a
np:Assertion
.
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_provenance
a
np:Provenance
.
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_assertion
{
miriam-gene:6911
a
ncit:C16612
.
lld:C0036439
a
ncit:C7057
.
dgn-gda:DGN690f51a6e3a47f98c337b7ffb48e9ed0
sio:SIO_000628
miriam-gene:6911
,
lld:C0036439
;
a
sio:SIO_001122
.
}
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_provenance
{
dgn-np:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_assertion
dcterms:description
"[This is the first report on SNPs of TBX6 gene in CS that suggests genetic variants of TBX6 gene is associated with CS and may play an important role in mediating susceptibility to developing CS in the Chinese Han population.]. 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:20228709
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP92002.RAdrhiVyfzT1-3rmbIFNjcmMajOnQMkwpYmdaICaEXTxg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}