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http://rdf.disgenet.org/nanopublications.trig#NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_assertion
a
np:Assertion
.
dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_provenance
a
np:Provenance
.
dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_publicationInfo
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np:PublicationInfo
.
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{
miriam-gene:401
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN9a602e93dcb063fa043bb9950093a915
sio:SIO_000628
miriam-gene:401
,
lld:C0000768
;
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.
}
dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_provenance
{
dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_assertion
dcterms:description
"[We hypothesize that CFEOM2 results from an analogous developmental defect to CFEOM1, one that affects both the superior and inferior divisions of the oculomotor nerve and their corresponding alpha motoneurons and extraocular muscles.]. 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:9683611
;
prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-20140225
pav:importedOn
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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
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dgn-np:NP605256.RAE6gsyO3rrGda8tYrFAnj51_1Ib26IgIPrzLWqY9g3IQ130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
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> , <
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> , <
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> ;
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<
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