Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion> ?p ?o ?g. }
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- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion type Assertion NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_head.
- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion description "[SPG11 mutations should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion evidence source_evidence_literature NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion SIO_000772 18439221 NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion wasDerivedFrom lhgdn-20090331 NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_assertion wasGeneratedBy ECO_0000203 NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.