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- NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_assertion type Assertion NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_head.
- NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_assertion description "[Here, we report the finding that MCPH1 primary microcephaly and PCC syndrome are allelic disorders, both having mutations in the MCPH1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_provenance.
- NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_assertion evidence source_evidence_literature NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_provenance.
- NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_assertion SIO_000772 15199523 NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_provenance.
- NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_assertion wasDerivedFrom befree-2016 NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_provenance.
- NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_assertion wasGeneratedBy ECO_0000203 NP448346.RAKXESMW_As4nSb3cMfniZUW8RJt7aF-HR-CfkTNR_dlY130_provenance.