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- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion type Assertion NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_head.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion wasGeneratedBy ECO_0000218 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion wasDerivedFrom uniprot-2016 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion SIO_000772 9529364 NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion evidence source_evidence_curated NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.
- NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_assertion description "[Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9695.RAv0l9IR89P10NrBIZZ2INkIMq3cXGDBFxsmIMXX13DNs130_provenance.