Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion> ?p ?o ?g. }
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- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion type Assertion NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_head.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion description "[In contrast to ALS, the risk of which is influenced by various factors other than SMN copy number itself, the association studies in LMND show a consistent finding that homozygous deletion of SMN2 may be specifically related to LMND, despite the small number of subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion evidence source_evidence_literature NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion SIO_000772 20947812 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion wasDerivedFrom befree-2016 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion wasGeneratedBy ECO_0000203 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.