Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion> ?p ?o ?g. }
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- NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion type Assertion NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_head.
- NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion description "[We performed p63 mutation analysis in a sample of 43 individuals and families affected with EEC syndrome, in 35 individuals affected with SHFM, and in three families with the EEC-like condition limb-mammary syndrome (LMS), which is characterized by ectrodactyly, cleft palate, and mammary-gland abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_provenance.
- NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion evidence source_evidence_literature NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_provenance.
- NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion SIO_000772 11462173 NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_provenance.
- NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion wasDerivedFrom befree-2016 NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_provenance.
- NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_assertion wasGeneratedBy ECO_0000203 NP324418.RAlVkAQYG9QwnItMPUtWNIHoFXr5wULI0co_GhQ4nJ9SE130_provenance.