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- NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_assertion type Assertion NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_head.
- NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_assertion description "[Meckel-Gruber syndrome type 3 (MKS3; OMIM 607361) is a severe autosomal recessive disorder characterized by bilateral polycystic kidney disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_provenance.
- NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_assertion evidence source_evidence_literature NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_provenance.
- NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_assertion SIO_000772 19211713 NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_provenance.
- NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_assertion wasDerivedFrom befree-20150227 NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_provenance.
- NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_assertion wasGeneratedBy ECO_0000203 NP960742.RAqTOeHPj___-Y1vydI_dHXyl-7a7XMG21NXvbM2S-eU4130_provenance.