Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_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." NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_assertion evidence source_evidence_literature NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_assertion SIO_000772 7727782 NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_assertion wasDerivedFrom befree-20140225 NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_assertion wasGeneratedBy ECO_0000203 NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717998.RAaWjsmtYI12M14P-6qVCdlWaYl71a19JSCMi51VgcEhs130_provenance.