Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion> ?p ?o ?g. }
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- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion type Assertion NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_head.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_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." NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion evidence source_evidence_literature NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion SIO_000772 20947812 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion wasDerivedFrom befree-20150227 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion wasGeneratedBy ECO_0000203 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.