Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_assertion> ?p ?o ?g. }
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- NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_assertion type Assertion NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_head.
- NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_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." NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_provenance.
- NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_assertion evidence source_evidence_literature NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_provenance.
- NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_assertion SIO_000772 9856479 NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_provenance.
- NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_assertion wasDerivedFrom befree-2016 NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_provenance.
- NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_assertion wasGeneratedBy ECO_0000203 NP1411095.RAfXfpxR7XufqOfB3Mc8GdZNWixSVTOUUacRuwgCf_ZTw130_provenance.