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- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion type Assertion NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_head.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion evidence source_evidence_literature NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion SIO_000772 10447258 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion wasDerivedFrom befree-2016 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.
- NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_assertion wasGeneratedBy ECO_0000203 NP260346.RAiuvpLJLNWh9_SBZVQ5i59RpI8_BBJqNvwPur7L-0Xh0130_provenance.