Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion> ?p ?o ?g. }
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- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion type Assertion NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_head.
- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_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." NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_provenance.
- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion evidence source_evidence_literature NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_provenance.
- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion SIO_000772 16912710 NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_provenance.
- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion wasDerivedFrom befree-20140225 NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_provenance.
- NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_assertion wasGeneratedBy ECO_0000203 NP213308.RABaUmtXRgSL8vrbd8wRpxeXAmjXI1b0A8dLsxy3oXPq8130_provenance.