Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion> ?p ?o ?g. }
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- NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion type Assertion NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_head.
- NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion description "[A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion evidence source_evidence_curated NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion SIO_000772 17646629 NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion wasDerivedFrom uniprot-2016 NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_assertion wasGeneratedBy ECO_0000218 NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.