Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP5059.RAosFamwgnubyKUj8rhomuzHNJLUs4p-gQ4gfcld9yDnE130_provenance.