Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion> ?p ?o ?g. }
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- NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion type Assertion NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_head.
- NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion description "[First, two thirds of nephrotic syndrome manifesting in the first year of life can be explained by mutations in 4 genes only (NPHS1, NPHS2, WT1, or LAMB2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_provenance.
- NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion evidence source_evidence_literature NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_provenance.
- NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion SIO_000772 17371932 NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_provenance.
- NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion wasDerivedFrom gad-20150221 NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_provenance.
- NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_assertion wasGeneratedBy ECO_0000203 NP106219.RANp8rji3NQgjVGWNc61mbccznMdy7h_inbzc3RDYh1IE130_provenance.