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http://rdf.disgenet.org/nanopublications.trig#NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI
> .
@prefix rdfs: <
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#
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_assertion
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np:hasProvenance
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a
np:Nanopublication
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dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_assertion
a
np:Assertion
.
dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_provenance
a
np:Provenance
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dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_publicationInfo
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np:PublicationInfo
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dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_assertion
{
miriam-gene:8048
a
ncit:C16612
.
lld:C0020608
a
ncit:C7057
.
dgn-gda:DGNa058e2212e21b1d43ea58a21d9e40cc7
sio:SIO_000628
miriam-gene:8048
,
lld:C0020608
;
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sio:SIO_001121
.
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dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_provenance
{
dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_assertion
dcterms:description
"[To investigate whether patients with ankyloglossia alone or in the presence of other craniofacial features including hypodontia or CLP might be caused by TBX22 mutations, we analyzed 45 Thai patients with isolated ankyloglossia, 2 unusual CPA families, and 282 non-syndromic Thai and UK patients with CLP.]. 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:21248356
;
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 .
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dgn-np:NP636014.RASlgrvJwHo7YQnxPHLhDNdrAJZQVmBEbXFgERzEkzsbI130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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> , <
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> , <
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> ;
pav:createdBy
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> ;
pav:version
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