Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion> ?p ?o ?g. }
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- NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion type Assertion NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_head.
- NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion wasGeneratedBy ECO_0000203 NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_provenance.
- NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion wasDerivedFrom befree-2016 NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_provenance.
- NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion SIO_000772 15735646 NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_provenance.
- NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion evidence source_evidence_literature NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_provenance.
- NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_assertion description "[Autosomal dominant mutations in the gene encoding the basic helix-loop-helix transcription factor Twist1 are associated with limb and craniofacial defects in humans with Saethre-Chotzen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482827.RAInh7Iv8icLJ2HfoC9v1exlQ2p8syD4UtSQXreHJQ30Q130_provenance.