Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion type Assertion NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_head.
- NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion description "[Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_provenance.
- NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion evidence source_evidence_curated NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_provenance.
- NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion SIO_000772 15805154 NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_provenance.
- NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion wasDerivedFrom uniprot-20130724 NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_provenance.
- NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_assertion wasGeneratedBy ECO_0000218 NP1018.RAd98wGGd79a9d7bsjtT3PvhLIwayxssxwjpC4yLlx_WI130_provenance.