Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion> ?p ?o ?g. }
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- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion type Assertion NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_head.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_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." NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion evidence source_evidence_literature NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion SIO_000772 11773000 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion wasDerivedFrom befree-20140225 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.
- NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_assertion wasGeneratedBy ECO_0000203 NP648522.RAh_FR2xh5-bvJMDkk936YP0QxT6iXGGQG9KtzePrMWRY130_provenance.