Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion> ?p ?o ?g. }
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- NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion type Assertion NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_head.
- NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion wasGeneratedBy ECO_0000203 NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_provenance.
- NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion wasDerivedFrom befree-20150227 NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_provenance.
- NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion SIO_000772 21668430 NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_provenance.
- NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion evidence source_evidence_literature NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_provenance.
- NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_assertion description "[Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968589.RAUBbN88DqZ0S0lBIYHfi_M9Sxkxc9kWdkIVEaRlrKvAM130_provenance.