@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE
> .
@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:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_head
{
this:
np:hasAssertion
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_assertion
;
np:hasProvenance
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_provenance
;
np:hasPublicationInfo
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_assertion
a
np:Assertion
.
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_provenance
a
np:Provenance
.
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_assertion
{
miriam-gene:57216
a
ncit:C16612
.
lld:C0033377
a
ncit:C7057
.
dgn-gda:DGN95c14700916337a4d61372613fe31505
sio:SIO_000628
miriam-gene:57216
,
lld:C0033377
;
a
sio:SIO_001121
.
}
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_provenance
{
dgn-np:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_assertion
dcterms:description
"[The patients with congenital disorders of the oblique muscles and with congenital elevation deficiencies other than Brown syndrome had relatives with ptosis, infantile esotropia, DRS, congenital abduction deficiency, and unspecified forms of 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:20535495
;
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:NP832701.RA4xkL--xKAEydQjITZs6de8ljxxN9q2hxlwZuv1_GPOE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+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" .
}