@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q
> .
@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/v4.0.0/void/
> .
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_head
{
this:
np:hasAssertion
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_assertion
;
np:hasProvenance
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_assertion
a
np:Assertion
.
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_provenance
a
np:Provenance
.
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNa2e39cc7efb1d69ecf611323184a4a3b
sio:SIO_000628
miriam-gene:3342
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_provenance
{
dgn-np:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_assertion
dcterms:description
"[Array-CGH analysis allowed for a higher rate of detection of chromosomal anomalies, and this determination is especially valuable in neonates with congenital anomalies of unknown etiology, or in cases in which karyotype results cannot be obtained.]. 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:25203518
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1218459.RAE7FzrlBragiSuJRo8nguDQMM8Odq8Fii6byo_ckV23Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:58+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}