Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_assertion description "[Our results demonstrated that some copy number changes thought to belong to early (MDM4 gain) or late stage (MYCN and E2F3 gain) of retinoblastoma are already present in retinoma at the same (for MDM4) or at lower (for MYCN and E2F3) copy number variation respect to retinoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_assertion evidence source_evidence_literature NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_assertion SIO_000772 18785023 NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_assertion wasDerivedFrom befree-20150227 NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_assertion wasGeneratedBy ECO_0000203 NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP551571.RAJ6x50IwpFEyyKUXOJ0U2oIlNfUcEvsaPcNaRL3E0P7k130_provenance.