Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion> ?p ?o ?g. }
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- NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion type Assertion NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_head.
- NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion description "[ARX mutation testing should be undertaken in children aged less than 1 year with Ohtahara syndrome and a movement disorder, and in infants with unexplained neurodegeneration, progressive white matter loss, and cortical atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_provenance.
- NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion evidence source_evidence_literature NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_provenance.
- NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion SIO_000772 19747203 NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_provenance.
- NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion wasDerivedFrom befree-2016 NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_provenance.
- NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_assertion wasGeneratedBy ECO_0000203 NP762648.RAi3_x7EPwyrvnXzl04QnT9PtiF-1REA8vKlo9FMBY4-w130_provenance.