Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion> ?p ?o ?g. }
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- NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion type Assertion NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_head.
- NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion wasGeneratedBy ECO_0000203 NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_provenance.
- NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion wasDerivedFrom befree-2016 NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_provenance.
- NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion SIO_000772 21091464 NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_provenance.
- NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion evidence source_evidence_literature NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_provenance.
- NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_assertion description "[Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853487.RAyRSN3yQDb3ixidMyQvVph3uBpT546g05h7yLjPUW7ZQ130_provenance.