Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion type Assertion NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_head.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion description "[Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion evidence source_evidence_literature NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion SIO_000772 9856479 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion wasDerivedFrom befree-2016 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.
- NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_assertion wasGeneratedBy ECO_0000203 NP1411096.RAY5QxFCh-g11RdnxXY4sXjFFy0_IlUqZSu0kLPSuDde4130_provenance.