Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion> ?p ?o ?g. }
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- NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion type Assertion NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_head.
- NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion description "[Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_provenance.
- NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion evidence source_evidence_curated NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_provenance.
- NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion SIO_000772 11078474 NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_provenance.
- NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion wasDerivedFrom ctd_human-2016 NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_provenance.
- NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_assertion wasGeneratedBy ECO_0000218 NP11003.RAsVXqk1E0mIf3M6AwhLjhvYfo72SjLbq-biYnGWyzNAg130_provenance.