@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s
> .
@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:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_head
{
this:
np:hasAssertion
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_assertion
a
np:Assertion
.
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_provenance
a
np:Provenance
.
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:83959
a
ncit:C16612
.
lld:C1562689
a
ncit:C7057
.
dgn-gda:DGN48765f49008aa5c4a84a66867c27c86b
sio:SIO_000628
miriam-gene:83959
,
lld:C1562689
;
a
sio:SIO_001121
.
}
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_provenance
{
dgn-np:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_assertion
dcterms:description
"[Identification of SLC4A11 as a candidate gene for congenital hereditary endothelial dystrophy with similar corneal endothelial defects as FECD and reduced mRNA expression of SLC4A11 in the endothelium of FECD cases suggested that this gene may also be involved in pathogenesis of FECD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:25007886
;
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:NP1199916.RAPJGTObKKDEk2KSBb4Rr32vDy_P-M20wWezioypacn_s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:50+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
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;
pav:authoredBy
<
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> , <
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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"v4.0.0" .
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