Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion> ?p ?o ?g. }
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- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion type Assertion NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_head.
- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion description "[We conclude that mutational analysis in LAMB2 should be considered in congenital nephrotic syndrome, if no mutations are found in NPHS1, NPHS2, or WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion evidence source_evidence_literature NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion SIO_000772 16912710 NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion wasDerivedFrom befree-20150227 NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_assertion wasGeneratedBy ECO_0000203 NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.