Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_assertion description "[Analysis of DCIS, IDC and LN components in the same patients revealed several consistent chromosomal changes present at all 3 sites: 1q, 7q, 8q, 16, 17, 19, 20q, 21q and 22q, the most frequent losses on 4q, 11q and 13q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_assertion evidence source_evidence_literature NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_assertion SIO_000772 10585588 NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_assertion wasDerivedFrom befree-2016 NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_assertion wasGeneratedBy ECO_0000203 NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP269108.RAa8NLOsFAcLzlgENNmkhw_rGtUeuJoxgwItVNHCIBKLc130_provenance.