Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion> ?p ?o ?g. }
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- NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion type Assertion NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_head.
- NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion description "[However, electroclinical descriptions in patients with ISSX carrying ARX mutations are scarce.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion evidence source_evidence_literature NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion SIO_000772 18468866 NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion wasDerivedFrom befree-20150227 NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_assertion wasGeneratedBy ECO_0000203 NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.