Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion type Assertion NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_head.
- NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion description "[Autosomal recessive spastic paraplegias (ARHSPs) usually have clinically complex phenotypes but the SPG5, SPG24, and SPG28 loci are considered to be associated with pure forms of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_provenance.
- NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion evidence source_evidence_literature NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_provenance.
- NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion SIO_000772 17503452 NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_provenance.
- NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion wasDerivedFrom befree-20150227 NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_provenance.
- NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_assertion wasGeneratedBy ECO_0000203 NP985071.RA764B8n0SLthIqrLba14Xx0CDU1VYo72_hBRNpGCt5sA130_provenance.