Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion> ?p ?o ?g. }
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- NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion type Assertion NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_head.
- NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion description "[Thirteen unrelated children with TBMN and five individuals with autosomal recessive Alport syndrome were examined for mutations in the 52 exons of COL4A3 and the 47 coding exons of COL4A4 using single-stranded conformation polymorphism (SSCP) analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_provenance.
- NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion evidence source_evidence_literature NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_provenance.
- NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion SIO_000772 17216251 NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_provenance.
- NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion wasDerivedFrom befree-2016 NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_provenance.
- NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_assertion wasGeneratedBy ECO_0000203 NP588242.RABNMYTKSMf9P2lpVEZMOGP6C6dDdPJ82nm0pjjPFHHc8130_provenance.