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- NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_assertion type Assertion NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_head.
- NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_assertion wasGeneratedBy ECO_0000218 NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_provenance.
- NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_assertion wasDerivedFrom uniprot-20130724 NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_provenance.
- NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_assertion SIO_000772 19603532 NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_provenance.
- NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_assertion evidence source_evidence_curated NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_provenance.
- NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_assertion description "[The mutational spectrum of holoprosencephaly-associated changes within the SHH gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5969.RAlGZgw6pSeJI0c0FX8rcz2FJ6O01_YM5GZDnAL1SsF6E130_provenance.