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- NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_assertion type Assertion NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_head.
- NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_assertion wasGeneratedBy ECO_0000218 NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_provenance.
- NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_assertion wasDerivedFrom ctd_human-2016 NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_provenance.
- NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_assertion SIO_000772 21091464 NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_provenance.
- NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_assertion evidence source_evidence_curated NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_provenance.
- NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_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." NP27730.RAtoROukf-N2TgrNfd6bVa1J7hOFo1rt_Zn1k_SfcNOyw130_provenance.