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- source_evidence_literature type ECO_0000212 NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP530562.RALcghhn17CfGFwf1EeH-uMu4kCbFE7m7fcSxF27oTnFE130_provenance.