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- source_evidence_literature type ECO_0000212 NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_assertion description "[Two novel mutations in the POU1F1 gene generate null alleles through different mechanisms leading to combined pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_assertion evidence source_evidence_literature NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_assertion SIO_000772 22010633 NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_assertion wasDerivedFrom befree-2016 NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_assertion wasGeneratedBy ECO_0000203 NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.
- befree-2016 importedOn "2016-02-19" NP932076.RA_DeHbEYq6E2mhQkbFyGPbCTfWNX7ZbtDo6AqbdLlAWo130_provenance.