Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_assertion description "[Loss of heterozygosity (LOH) for p73 was observed in 19% (28/151) of informative cases which included 92 mass-screening (MS) tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_assertion evidence source_evidence_literature NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_assertion SIO_000772 10023682 NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_assertion wasDerivedFrom befree-20150227 NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_assertion wasGeneratedBy ECO_0000203 NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP952526.RA7xkZvT1540NlnQ8M1HxiWnlp_6Rslp0s5NnELo4ZQrY130_provenance.