@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ
> .
@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:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_head
{
this:
np:hasAssertion
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_assertion
;
np:hasProvenance
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_assertion
a
np:Assertion
.
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_provenance
a
np:Provenance
.
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_assertion
{
miriam-gene:744
a
ncit:C16612
.
lld:C0206115
a
ncit:C7057
.
dgn-gda:DGNb34625d997d527ea6c6d7cae33805604
sio:SIO_000628
miriam-gene:744
,
lld:C0206115
;
a
sio:SIO_001121
.
}
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_provenance
{
dgn-np:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_assertion
dcterms:description
"[We performed a large scale bioinformatic analysis to identify orthologs of the Rv0805 protein and identified many eukaryotic genes that included the human 239FB gene present in the region deleted in the WAGR syndrome.]. 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:19004815
;
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:NP690069.RALdFK86LK7gmCFcjOfF4gH6mlVZriXtkZhrItwJx2MWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}