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- source_evidence_literature type ECO_0000212 NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_assertion description "[Mutation analysis of the ALX4 gene in three unrelated FPP families without the MSX2 mutation identified mutations in two families, indicating that mutations in ALX4 could be responsible for these skull defects and suggesting further genetic heterogeneity of FPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_assertion evidence source_evidence_literature NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_assertion SIO_000772 11106354 NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_assertion wasDerivedFrom befree-2016 NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_assertion wasGeneratedBy ECO_0000203 NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.
- befree-2016 importedOn "2016-02-19" NP302228.RABZoc-Q-CYRnuUHuYXqy3LD-9AhCUENtYOI0UYukkYXg130_provenance.