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- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_assertion type Assertion NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_head.
- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_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." NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_provenance.
- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_assertion evidence source_evidence_literature NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_provenance.
- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_assertion SIO_000772 11773000 NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_provenance.
- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_assertion wasDerivedFrom befree-20140225 NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_provenance.
- NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_assertion wasGeneratedBy ECO_0000203 NP221768.RAeOkAYeyHyQShDmlsur_95xSnE7FjHNkmz1GYbHnPTKs130_provenance.