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- NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_assertion type Assertion NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_head.
- NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_assertion wasGeneratedBy ECO_0000203 NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_provenance.
- NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_assertion wasDerivedFrom befree-2016 NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_provenance.
- NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_assertion SIO_000772 8981947 NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_provenance.
- NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_assertion evidence source_evidence_literature NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_provenance.
- NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_assertion description "[We identified a novel heterozygous Gly166Cys mutation in TIMP3 in all affected individuals and provide strong evidence for an autosomal dominant inheritance of the SFD phenotype in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365005.RAo3ykwJiQsLbKHodPOzitw301zkTUcswdQ5BcXvbIKow130_provenance.