Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion> ?p ?o ?g. }
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- NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion type Assertion NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_head.
- NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion description "[Our results show a high incidence of SMN1 gene deletion in adult-onset SMA patients indicating that SMN1 is the autosomal recessive adult SMA-causing gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_provenance.
- NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion evidence source_evidence_literature NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_provenance.
- NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion SIO_000772 14586604 NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_provenance.
- NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion wasDerivedFrom befree-2016 NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_provenance.
- NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_assertion wasGeneratedBy ECO_0000203 NP418765.RA6Dc3fzmSn5VQp-H-SmxHHljwt_bGltli1UcaEtP2HMA130_provenance.