Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_assertion> ?p ?o ?g. }
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- NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_assertion type Assertion NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_head.
- NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_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." NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_provenance.
- NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_assertion evidence source_evidence_curated NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_provenance.
- NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_assertion SIO_000772 11078474 NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_provenance.
- NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_assertion wasDerivedFrom ctd_human-20150221 NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_provenance.
- NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_assertion wasGeneratedBy ECO_0000218 NP15073.RARYWVVWPrGh8rBmNFMKZDpwnfmwcECKqtGogoVGbdhaE130_provenance.