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- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion type Assertion NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_head.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_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." NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion evidence source_evidence_literature NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion SIO_000772 16912710 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion wasDerivedFrom befree-20150227 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.
- NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_assertion wasGeneratedBy ECO_0000203 NP958121.RAEw_uB-PRI9Dkh-c94_C6bP8OtnhuzDeqBttqwtN5r_s130_provenance.