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- NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_assertion type Assertion NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_head.
- NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_assertion wasGeneratedBy ECO_0000203 NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_provenance.
- NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_assertion wasDerivedFrom befree-2016 NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_provenance.
- NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_assertion SIO_000772 11159940 NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_provenance.
- NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_assertion evidence source_evidence_literature NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_provenance.
- NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_assertion description "[Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP305672.RAELGo_elix9gdQmYAoLUx2gvUhTOMdfJHE8a0mFz5U30130_provenance.