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- source_evidence_literature type ECO_0000212 NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP189961.RA10bfGCHKQoatl6xJALbtdrYDiLwpVOp6zCbMTdCmLX8130_provenance.