Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion> ?p ?o ?g. }
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- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion type Assertion NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_head.
- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion description "[Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_provenance.
- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion evidence source_evidence_literature NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_provenance.
- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion SIO_000772 23453666 NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_provenance.
- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion wasDerivedFrom befree-2016 NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_provenance.
- NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_assertion wasGeneratedBy ECO_0000203 NP1057100.RAQEf4zU_EV76sE56aTNwV2kc_x0ea98keIVaQSketUSc130_provenance.