Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion type Assertion NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_head.
- NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion description "[ The results demonstrate that NPHS2 mutations are also present in Chinese sporadic SRNS. Our investigation supports the necessity of searching for mutations in NPHS2 in Chinese children with sporadic SRNS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_provenance.
- NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion evidence source_evidence_literature NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_provenance.
- NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion SIO_000772 15769810 NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_provenance.
- NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion wasDerivedFrom gad-20130706 NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_provenance.
- NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_assertion wasGeneratedBy ECO_0000203 NP53778.RAv5wSccVggteFzwS68T6ffN4FeETa8eVv1YEnS_F1O8Q130_provenance.