Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion> ?p ?o ?g. }
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- NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion type Assertion NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_head.
- NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion description "[CHARGE syndrome is an autosomal dominant multisystem disorder caused by mutation in the CHD7 gene, encoding chromodomain helicase DNA-binding protein 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_provenance.
- NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion evidence source_evidence_curated NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_provenance.
- NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion SIO_000772 21158681 NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_provenance.
- NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion wasDerivedFrom uniprot-20130724 NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_provenance.
- NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_assertion wasGeneratedBy ECO_0000218 NP1101.RAv7PazrBIAMHyXM9Ey78Nzq2u8Jmw5bXXNH6Ip8CmGj4130_provenance.