Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion type Assertion NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_head.
- NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion description "[New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_provenance.
- NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion evidence source_evidence_literature NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_provenance.
- NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion SIO_000772 19034539 NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_provenance.
- NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion wasDerivedFrom gad-20150221 NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_provenance.
- NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_assertion wasGeneratedBy ECO_0000203 NP134990.RALRdL2d-yJx4lEx8ME7kHOhoINctsXCwXbSQvPWMAsD0130_provenance.