@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U
> .
@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:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_head
{
this:
np:hasAssertion
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_assertion
;
np:hasProvenance
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_provenance
;
np:hasPublicationInfo
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_assertion
a
np:Assertion
.
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_provenance
a
np:Provenance
.
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_assertion
{
miriam-gene:3236
a
ncit:C16612
.
lld:C0009081
a
ncit:C7057
.
dgn-gda:DGN209d2e633898c02820d27837aa8c10b5
sio:SIO_000628
miriam-gene:3236
,
lld:C0009081
;
a
sio:SIO_001121
.
}
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_provenance
{
dgn-np:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_assertion
dcterms:description
"[To determine whether HOXD10 is involved in the etiology of idiopathic clubfoot, HOXD10 coding and 5' and 3' untranslated regions were resequenced in 190 patients (177 with clubfoot, 10 with sporadic vertical talus, and 3 with both clubfoot and vertical talus), and 160 ethnically matched control subjects.]. 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:17417092
;
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:NP704550.RAJp4k32u-rBkeOlcLcEcKbp5cVQO-vMmvkxDs-uXH99U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}