Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion type Assertion NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_head.
- NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion description "[A genetic mutation within its MSP domain, P56S, was identified in familial forms of motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_provenance.
- NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion evidence source_evidence_literature NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_provenance.
- NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion SIO_000772 20207736 NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_provenance.
- NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion wasDerivedFrom befree-20150227 NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_provenance.
- NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_assertion wasGeneratedBy ECO_0000203 NP954406.RAbT9ZLgiUdDBoZn78Dt2A5okzKQSd1gx5W1T6hJydT_k130_provenance.