Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_assertion description "[We found only one mutation of the N-ras gene that was a 2-bp substitution of GGT(Gly) to GTC(Val) at codon 13 among 22 t(1;19)-ALL cases and five cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_assertion evidence source_evidence_literature NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_assertion SIO_000772 7727782 NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_assertion wasDerivedFrom befree-20150227 NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_assertion wasGeneratedBy ECO_0000203 NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1010243.RAVoV43Q9j4a2-l8JFKFD5Dm5-nK9c3hHWYsQPQFgKmP4130_provenance.