Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion type Assertion NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_head.
- NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion description "[Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the survival motor neuron gene (SMN), which exists in 2 nearly identical copies (SMN1 and SMN2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_provenance.
- NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion evidence source_evidence_literature NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_provenance.
- NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion SIO_000772 17761649 NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_provenance.
- NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion wasDerivedFrom befree-20140225 NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_provenance.
- NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_assertion wasGeneratedBy ECO_0000203 NP442172.RAj5AzAJajUjSv0b_WeGz3WyAcm2vTugWmtKpmNNfSNzc130_provenance.