@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998
> .
@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:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_head
{
this:
np:hasAssertion
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_assertion
;
np:hasProvenance
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_provenance
;
np:hasPublicationInfo
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_assertion
a
np:Assertion
.
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_provenance
a
np:Provenance
.
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_assertion
{
miriam-gene:57216
a
ncit:C16612
.
lld:C0005745
a
ncit:C7057
.
dgn-gda:DGNb3f609fde9d32ec51cf46910a3deff06
sio:SIO_000628
miriam-gene:57216
,
lld:C0005745
;
a
sio:SIO_001121
.
}
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_provenance
{
dgn-np:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_assertion
dcterms:description
"[Clinical features include synkinesis of the eyelids with the orbicularis oris causing synkinetic ptosis, recurrent paralytic ectropion, paralysis of facial muscles of expression with dry eye, hyperlacrimation (crocodile tears), and transient strabismus.]. 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:16191801
;
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:NP215201.RAHd-xuoywMXuCLdMoMnPEOaM5OJVf17j_gfkUpriZ998130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}