@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc
> .
@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:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_head
{
this:
np:hasAssertion
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_assertion
;
np:hasProvenance
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_assertion
a
np:Assertion
.
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_provenance
a
np:Provenance
.
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_assertion
{
miriam-gene:643915
a
ncit:C16612
.
lld:C0035304
a
ncit:C7057
.
dgn-gda:DGN50e95fee1a02d6152048f00bef962544
sio:SIO_000628
miriam-gene:643915
,
lld:C0035304
;
a
sio:SIO_001121
.
}
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_provenance
{
dgn-np:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_assertion
dcterms:description
"[Thus, inactivation of MRG4 by gene targeting resulted in a retinal degeneration phenotype quite different from that previously seen in the TG, attesting to the multiplicity of MRG4 function, in addition to the importance of this protein for normal retinal function.]. 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:17174953
;
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:NP581410.RA713iFbQ54NSTiKpCjzkOMZjhWojlFMj6fJ1lV3X0zSc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}