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- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion type Assertion NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_head.
- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion description "[We have identified a homozygous missense mutation in the RAD51C gene in a consanguineous family with multiple severe congenital abnormalities characteristic of FA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_provenance.
- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion evidence source_evidence_literature NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_provenance.
- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion SIO_000772 20400963 NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_provenance.
- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion wasDerivedFrom befree-20150227 NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_provenance.
- NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_assertion wasGeneratedBy ECO_0000203 NP663814.RAoR0Yfgaylv_lYlR0z7r7HfnKxfHdYZRiRI-d_te6K3o130_provenance.