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- NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_assertion type Assertion NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_head.
- NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_assertion description "[The X-linked recessive centronuclear/myotubular myopathy (XLR-CNM/MTM1), a severe neonatal disorder characterized by generalized hypotonia, muscle weakness and primary asphyxia, has recently been mapped to Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_provenance.
- NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_assertion evidence source_evidence_literature NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_provenance.
- NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_assertion SIO_000772 1822801 NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_provenance.
- NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_assertion wasDerivedFrom befree-2016 NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_provenance.
- NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_assertion wasGeneratedBy ECO_0000203 NP652316.RATcQO1LF40or_hz1jdZeSd7cs2hqvJUq6h9cIPM17wkE130_provenance.