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- source_evidence_literature type ECO_0000212 NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP616252.RAHcE0nObzKBcbr0CCqyxFn_no1ibYu89tJJE4uF4kJtw130_provenance.