Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- befree-2016 importedOn "2016-02-19" NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_assertion wasGeneratedBy ECO_0000203 NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_assertion wasDerivedFrom befree-2016 NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_assertion SIO_000772 14594802 NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_assertion evidence source_evidence_literature NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.
- NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_assertion description "[Two hereditary AML predisposition syndromes may therefore intersect via LEF-1, potentially linking them to more generalized cancer mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418950.RArwcXG9G7x2EFW8GLuFTj326M1ouH9v4FuVZEML7N8cw130_provenance.