Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion> ?p ?o ?g. }
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- NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion type Assertion NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_head.
- NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion description "[The majority of the XLA disease-causing mutations in the Btk PH domain were found at positions having significant mutual information, indicating that there are covariant constraints for both structure and function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_provenance.
- NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion evidence source_evidence_literature NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_provenance.
- NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion SIO_000772 15082835 NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_provenance.
- NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion wasDerivedFrom befree-2016 NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_provenance.
- NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_assertion wasGeneratedBy ECO_0000203 NP439711.RAmZiNDt5xNnJP_fLHpE2UcmdbbcjeRK_say4XJFkzIOs130_provenance.