Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion> ?p ?o ?g. }
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- NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion type Assertion NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_head.
- NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion description "[FOXC2 represents the second known gene to result in hereditary lymphedema, and LD is only the second hereditary disorder known to be caused by a mutation in a forkhead-family gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_provenance.
- NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion evidence source_evidence_literature NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_provenance.
- NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion SIO_000772 11078474 NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_provenance.
- NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion wasDerivedFrom befree-20140225 NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_provenance.
- NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_assertion wasGeneratedBy ECO_0000203 NP167546.RAc-vkhZysp-w84KdBFqZGOnN15Ornom1qFTPGRPT_a_A130_provenance.