@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U
> .
@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 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:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_head
{
this:
np:hasAssertion
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion
;
np:hasProvenance
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_provenance
;
np:hasPublicationInfo
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion
a
np:Assertion
.
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_provenance
a
np:Provenance
.
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion
{
miriam-gene:4626
a
ncit:C16612
.
lld:C0009081
a
ncit:C7057
.
dgn-gda:DGNb31344c5cd2475f2f451e6df302567fa
sio:SIO_000628
miriam-gene:4626
,
lld:C0009081
;
a
sio:SIO_001122
.
}
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_provenance
{
dgn-np:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_assertion
dc:description
"[This study further differentiates congenital idiopathic clubfoot as distinct from other complex genetic syndromes that can present with similar deformities, and thus facilitates further research to improve the clinical diagnosis and treatment of congenital idiopathic clubfoot.]. 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:20357587
;
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:NP83959.RAa4m_f1AhUX2Dfva6jJKxLtp2nCLskL2PhZQL13rSK-U130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:41+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}