Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_assertion description "[AID transcripts, including a splice variant, were common to both unmutated or mutated VH genes in mantle cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_assertion evidence source_evidence_literature NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_assertion SIO_000772 14551145 NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_assertion wasDerivedFrom lhgdn-20090331 NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_assertion wasGeneratedBy ECO_0000203 NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP201757.RA5XKiymHaqTzBwyksmfaJLF0DUxZAcuZ94Jtm-gyH6ys130_provenance.