Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion> ?p ?o ?g. }
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- NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion type Assertion NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_head.
- NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion description "[Of the 38 Hungarian patients screened, seven carried NPHS2 mutations on both alleles, of whom two-diagnosed with proteinuria through school screening programs at the age of 9.7 and 14�years, respectively-did not develop nephrotic syndrome in childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_provenance.
- NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion evidence source_evidence_literature NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_provenance.
- NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion SIO_000772 23242530 NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_provenance.
- NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion wasDerivedFrom befree-20150227 NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_provenance.
- NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_assertion wasGeneratedBy ECO_0000203 NP783728.RA-ACGIBvUiL-HhIEOIu-IUhwaA3SASpfbMbKmS-4m_LU130_provenance.