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- NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_assertion type Assertion NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_head.
- NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_assertion wasGeneratedBy ECO_0000203 NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_provenance.
- NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_assertion wasDerivedFrom befree-2016 NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_provenance.
- NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_assertion SIO_000772 15459175 NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_provenance.
- NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_assertion evidence source_evidence_literature NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_provenance.
- NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_assertion description "[RAI1 has been recently suggested as a major gene for majority of the SMS phenotypes, but its role in the full spectrum of the phenotype remains unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462750.RAHdTPjmOt12cr2Ah__FSADKORo-QkhnGTB9qWY8rC4Bo130_provenance.