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- source_evidence_literature type ECO_0000212 NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_assertion description "[Novel mutations in SAR1B and MTTP genes in Tunisian children with chylomicron retention disease and abetalipoproteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_assertion evidence source_evidence_literature NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_assertion SIO_000772 23043934 NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_assertion wasDerivedFrom befree-20150227 NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_assertion wasGeneratedBy ECO_0000203 NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP901822.RAw5rDVEw_FzNh6TY8KwM0VKcFPQRPqH6D0LCXU48MvQE130_provenance.