Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_assertion description "[No other gene is present in the wasted deletion, and transgenic studies have shown that the phenotype is due to loss of eEF1A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_assertion evidence source_evidence_literature NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_assertion SIO_000772 19909265 NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_assertion wasDerivedFrom befree-2016 NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_assertion wasGeneratedBy ECO_0000203 NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.
- befree-2016 importedOn "2016-02-19" NP775418.RA5q7bju3zJpG_eAYFCCMrTEjn8GP13xwJw7_E9HBJ5tM130_provenance.