Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion> ?p ?o ?g. }
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- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion type Assertion NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_head.
- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion wasGeneratedBy ECO_0000203 NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_provenance.
- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion wasDerivedFrom befree-20140225 NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_provenance.
- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion SIO_000772 17236141 NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_provenance.
- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion evidence source_evidence_literature NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_provenance.
- NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_assertion description "[Polyalanine expansions in HOXD13 cause synpolydactyly, whereas amino acid substitutions in the homeodomain are associated with brachydactyly types D and E. We describe two large Han Chinese families with different limb malformations, one with syndactyly type V and the other with limb features overlapping brachydactyly types A4, D, and E and mild syndactyly of toes 2 and 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451459.RAsp0WdtD75oFidLmA7TdsFzjMgPIXpVZok0zKSulbKcc130_provenance.