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- NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_assertion type Assertion NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_head.
- NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_assertion description "[MYH9-related disease (MYH9-RD) is a rare autosomal dominant genetic syndrome characterized by congenital thrombocytopenia associated with the risk of developing progressive nephropathy, sensorineural deafness, and presenile cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_provenance.
- NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_assertion evidence source_evidence_literature NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_provenance.
- NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_assertion SIO_000772 22558294 NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_provenance.
- NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_assertion wasDerivedFrom befree-20140225 NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_provenance.
- NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_assertion wasGeneratedBy ECO_0000203 NP733155.RA2bFpEe1ghZo5tz18LzGKSClCA3sXNzviX0s3bIxo4l0130_provenance.