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- NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_assertion type Assertion NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_head.
- NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_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." NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_assertion evidence source_evidence_literature NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_assertion SIO_000772 10447258 NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_assertion wasDerivedFrom befree-20150227 NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_assertion wasGeneratedBy ECO_0000203 NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.