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- source_evidence_literature type ECO_0000212 NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP835565.RA4K21q4sn27ttS8YQ6l_23EC1Cm0TGwEmu8snbkT5NQc130_provenance.