Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_assertion description "[We report on a 26-month-old boy with developmental delay and multiple congenital anomalies, including many features suggestive of either branchiootorenal syndrome (BOR) or oculoauriculovertebral spectrum (OAVS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_assertion evidence source_evidence_literature NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_assertion SIO_000772 18666230 NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_assertion wasDerivedFrom befree-20140225 NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_assertion wasGeneratedBy ECO_0000203 NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP323812.RA6uOtaZqp65yrkqZ5vfFuTKMel9mP3gaeE9Afl6m4kfg130_provenance.