@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk
> .
@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:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_head
{
this:
np:hasAssertion
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_assertion
;
np:hasProvenance
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_provenance
;
np:hasPublicationInfo
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_assertion
a
np:Assertion
.
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_provenance
a
np:Provenance
.
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_assertion
{
miriam-gene:7045
a
ncit:C16612
.
lld:C1275685
a
ncit:C7057
.
dgn-gda:DGN9158ad060a557987af09c5a210f6201a
sio:SIO_000628
miriam-gene:7045
,
lld:C1275685
;
a
sio:SIO_001121
.
}
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_provenance
{
dgn-np:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_assertion
dcterms:description
"[To our knowledge, this is the first case report of clinical, histopathological, microscopic features of ACD in young patient of Indian origin with absence of BIGH3 gene treated with FALK with IntraLase Femtosecond Laser for donor and recipient cuts.]. 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:19657278
;
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:NP192991.RAj6_fV51PwRvXLDZUtL63z-FOrYMQSSgjhWv58APDDQk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}