@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E
> .
@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:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_head
{
this:
np:hasAssertion
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_assertion
;
np:hasProvenance
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_provenance
;
np:hasPublicationInfo
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_assertion
a
np:Assertion
.
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_provenance
a
np:Provenance
.
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_assertion
{
miriam-gene:54113
a
ncit:C16612
.
lld:C0042580
a
ncit:C7057
.
dgn-gda:DGN80e3e7c5858bfbf9b2f2a9db74bcb6af
sio:SIO_000628
miriam-gene:54113
,
lld:C0042580
;
a
sio:SIO_001121
.
}
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_provenance
{
dgn-np:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_assertion
dcterms:description
"[It is likely that over the next few years VUR genes will be mapped and, once identified, the challenge will be to understand how changes in the expression of these genes lead to the underlying defect in VUR.]. 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:10976387
;
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:NP772395.RAcmfolp0vUAxGWDU2sA-ELpt9u0eqWBfbO1b5Aj7y66E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}