@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_head
{
this:
np:hasAssertion
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_assertion
;
np:hasProvenance
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_assertion
a
np:Assertion
.
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_provenance
a
np:Provenance
.
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_assertion
{
miriam-gene:1714
a
ncit:C16612
.
lld:C0741916
a
ncit:C7057
.
dgn-gda:DGN852f152608fa3dd7f6a08a459518f1e6
sio:SIO_000628
miriam-gene:1714
,
lld:C0741916
;
a
sio:SIO_001121
.
}
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_provenance
{
dgn-np:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_assertion
dcterms:description
"[It would also be advisable that children with isolated CTD should be carefully examined to detect the other morphologic abnormalities of DGA and VCFS, or CATCH 22 (cardiac defects, abnormal facies, thymic hypoplasia/aplasia, cleft palate, hypocalcemia, and 22q11 deletion).]. 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:9216164
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP353273.RAAuG7AOOxfPQdTSe6C1ElK3j7pFWexyEZ8vCEwJInqI4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:03+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}