Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion> ?p ?o ?g. }
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- NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion type Assertion NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_head.
- NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion description "[The clinically unaffected parents were heterozygous for the mutations, suggesting that both COL7A1 gene defects were recessively inherited disease-causing mutations that are silent in heterozygous carriers but in combination can severely interfere with the dermal-epidermal adhesion and lead to severe EBD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_provenance.
- NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion evidence source_evidence_literature NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_provenance.
- NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion SIO_000772 9284109 NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_provenance.
- NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion wasDerivedFrom befree-2016 NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_provenance.
- NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_assertion wasGeneratedBy ECO_0000203 NP1379753.RAbnmuF9i9p9Kg0Xy81CTHLW06fgLy4TNNzMf1W70fpZs130_provenance.