Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion> ?p ?o ?g. }
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- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion type Assertion NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_head.
- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_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." NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_provenance.
- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion evidence source_evidence_literature NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_provenance.
- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion SIO_000772 16912710 NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_provenance.
- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion wasDerivedFrom befree-20140225 NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_provenance.
- NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_assertion wasGeneratedBy ECO_0000203 NP570295.RAREjFCNVU_oroIEe-tD_C1KdceyMHtSFpDc4SGYm0Opw130_provenance.