@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU
> .
@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:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_head
{
this:
np:hasAssertion
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_assertion
;
np:hasProvenance
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_provenance
;
np:hasPublicationInfo
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_assertion
a
np:Assertion
.
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_provenance
a
np:Provenance
.
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_assertion
{
miriam-gene:1714
a
ncit:C16612
.
lld:C0012236
a
ncit:C7057
.
dgn-gda:DGNdc939df05a6506abb3d6fc019af088b1
sio:SIO_000628
miriam-gene:1714
,
lld:C0012236
;
a
sio:SIO_001121
.
}
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_provenance
{
dgn-np:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_assertion
dcterms:description
"[This study also suggested that systematic approaches with several small DNA probes along the DGCR could help to dissect the complex phenotypes associated with the DiGeorge syndrome, such as cardiac defects, abnormal faces, thymic hypoplasia, cleft palate, and hypocalcemia, etc.]. 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:10102575
;
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:NP222705.RATTF5_-JpxnZtaQJ7e9orf2r-2N1ebvCGVpEUGrCcrNU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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: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" .
}