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- NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_assertion type Assertion NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_head.
- NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_assertion description "[Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_provenance.
- NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_assertion evidence source_evidence_literature NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_provenance.
- NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_assertion SIO_000772 25504045 NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_provenance.
- NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_assertion wasDerivedFrom befree-2016 NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_provenance.
- NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_assertion wasGeneratedBy ECO_0000203 NP1247973.RAJKjL9t7f3CpJHnbYGzv1jsLKAsH8GUXqDfyLpLugJgE130_provenance.