Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion> ?p ?o ?g. }
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- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion type Assertion NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_head.
- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion description "[Mutations in both alleles of the tumour suppressor gene coding for merlin/schwannomin, an ERM family protein, cause the hereditary disease neurofibromatosis type 2 (NF2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_provenance.
- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion evidence source_evidence_literature NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_provenance.
- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion SIO_000772 11773000 NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_provenance.
- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion wasDerivedFrom befree-20140225 NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_provenance.
- NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_assertion wasGeneratedBy ECO_0000203 NP599592.RAcO2bzGVxcukBBvaexX-bi2jx8Lm9H3Jj2sF6-n-bzYw130_provenance.