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- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion type Assertion NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_head.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion wasGeneratedBy ECO_0000203 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion wasDerivedFrom befree-20150227 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion SIO_000772 23171239 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion evidence source_evidence_literature NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.