Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_assertion description "[Clonal patterns were found in 3 of 10 cases of syncytial variant of NSHD, including 2 of 3 (67%) CD20+ cases and 1 of 7 (14%) B-cell antigen-negative cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_assertion evidence source_evidence_literature NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_assertion SIO_000772 7572792 NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_assertion wasDerivedFrom befree-20140225 NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_assertion wasGeneratedBy ECO_0000203 NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP791767.RA8mT2OsrEak-0dKze_k927fu0LaLaAooTGiKbhLY88jM130_provenance.