Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_assertion> ?p ?o ?g. }
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- NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_assertion type Assertion NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_head.
- NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_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." NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_provenance.
- NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_assertion evidence source_evidence_literature NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_provenance.
- NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_assertion SIO_000772 11078474 NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_provenance.
- NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_assertion wasDerivedFrom befree-2016 NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_provenance.
- NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_assertion wasGeneratedBy ECO_0000203 NP300435.RA_ZeA9Yb4-7y8hbpqteB7q8Yn8DiV1XYbZ2mbLYgXh4E130_provenance.