@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI
> .
@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:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_head
{
this:
np:hasAssertion
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_assertion
;
np:hasProvenance
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_assertion
a
np:Assertion
.
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_provenance
a
np:Provenance
.
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_assertion
{
miriam-gene:1296
a
ncit:C16612
.
lld:C0016781
a
ncit:C7057
.
dgn-gda:DGNff75be74b7814d123ee4c4b7bae9098a
sio:SIO_000628
miriam-gene:1296
,
lld:C0016781
;
a
sio:SIO_001121
.
}
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_provenance
{
dgn-np:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_assertion
dcterms:description
"[This group of conditions includes Fuchs' endothelial dystrophy of the cornea (FECD), one of the commonest indications for corneal transplantation performed in developed countries, posterior polymorphous dystrophy (PPCD) and the congenital hereditary endothelial dystrophies (CHED).]. 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:11689488
;
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:NP429292.RAu4N1MNTUGabU16Zu7J2ImmNw6qgvXS6rB8fceo1nfRI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}