@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion
;
np:hasProvenance
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_provenance
;
np:hasPublicationInfo
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion
a
np:Assertion
.
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_provenance
a
np:Provenance
.
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion
{
miriam-gene:157570
a
ncit:C16612
.
lld:C0392475
a
ncit:C7057
.
dgn-gda:DGN6b05f3fbf1e80aaf9de20d79894ee9af
sio:SIO_000628
miriam-gene:157570
,
lld:C0392475
;
a
sio:SIO_001121
.
}
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_provenance
{
dgn-np:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_assertion
dcterms:description
"[Since ESCO2 has been identified as the gene defective in the rare autosomal recessive cohesinopathy Roberts syndrome (RBS), cells from RBS patients can be used to elucidate the role of ESCO2.]. 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:19738907
;
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:NP638589.RApWwN_1qqmfcDyxQxkyYycsJfgctwOwHlZyTHJQirjMY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:25+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
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dgn-void:disgenetrdf
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}