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- NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_assertion type Assertion NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_head.
- NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_assertion wasGeneratedBy ECO_0000203 NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_provenance.
- NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_assertion wasDerivedFrom befree-2016 NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_provenance.
- NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_assertion SIO_000772 15007723 NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_provenance.
- NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_assertion evidence source_evidence_literature NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_provenance.
- NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_assertion description "[A TSC2-PKD1 contiguous gene syndrome caused by chromosomal microdeletions disrupting both the TSC2 and PKD1 genes has been identified in patients with TSC and early-onset severe ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434693.RAYwmLRMZ4LZ8AxnfF2AwG9KBTl5npS3KThaQFA67Vgus130_provenance.