Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion> ?p ?o ?g. }
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- NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion type Assertion NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_head.
- NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion description "[High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_provenance.
- NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion evidence source_evidence_literature NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_provenance.
- NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion SIO_000772 17035675 NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_provenance.
- NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion wasDerivedFrom befree-20150227 NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_provenance.
- NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_assertion wasGeneratedBy ECO_0000203 NP710048.RAQIgeiGhX3DONSKnMlnwpA8ztYTPR0S2mVeOXDLV9RNw130_provenance.