Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_assertion description "[MM shows frequent genetic inactivation of tumor suppressor genes of p16(INK4a)/p14(ARF) and neurofibromatosis type 2 (NF2) which encodes Merlin, and epigenetic inactivation of RASSF1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_assertion evidence source_evidence_literature NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_assertion SIO_000772 19793348 NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_assertion wasDerivedFrom befree-20150227 NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_assertion wasGeneratedBy ECO_0000203 NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP861882.RAu98fWy19vRZJM4RP4ffzjQbnADpxJXXS0Bz0g8-M69M130_provenance.