Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion type Assertion NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_head.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion description "[Determination of the sequence of the SNX10 gene is warranted in molecularly undefined patients with recessive 'pure' osteopetrosis of infancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion evidence source_evidence_literature NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion SIO_000772 22499339 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion wasDerivedFrom befree-20140225 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.
- NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_assertion wasGeneratedBy ECO_0000203 NP169902.RA3iI2vKGHL-J406C08z4FJ_YgTfphCNjv92hlDOsTGCY130_provenance.