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- source_evidence_literature type ECO_0000212 NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_assertion description "[Our observation demonstrates that FMR2 gene deletions may contribute to the FRAXE phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_assertion evidence source_evidence_literature NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_assertion SIO_000772 21739600 NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_assertion wasDerivedFrom befree-20150227 NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_assertion wasGeneratedBy ECO_0000203 NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412846.RAfXKDcoHEpefCc90E-GnDPaKVukPXNvg1DSzjgjjYGy4130_provenance.