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- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion type Assertion NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_head.
- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_provenance.
- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion evidence source_evidence_literature NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_provenance.
- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion SIO_000772 24754450 NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_provenance.
- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion wasDerivedFrom befree-2016 NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_provenance.
- NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_assertion wasGeneratedBy ECO_0000203 NP1175637.RAD15FQwTI7WmOkaS1ZUQqoIb9tHnoYVnhGbac6lpgl_Q130_provenance.