Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion> ?p ?o ?g. }
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- NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion type Assertion NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_head.
- NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion description "[The chromatin-associated protein ATRX was originally identified because mutations in the ATRX gene cause a severe form of syndromal X-linked mental retardation associated with alpha-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_provenance.
- NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion evidence source_evidence_literature NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_provenance.
- NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion SIO_000772 17609377 NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_provenance.
- NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion wasDerivedFrom befree-20150227 NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_provenance.
- NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_assertion wasGeneratedBy ECO_0000203 NP257460.RAosB6cag7gmSJuJQBTchfqsfAzN99Zq6uGrRzX55N2Mg130_provenance.