Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_assertion description "[IDH1 and IDH2 mutations were found in four (2.0%) and ten (5.0%) AML and in two (2.4%) and three (3.6%) MDS cases, but not in other patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_assertion evidence source_evidence_literature NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_assertion SIO_000772 21997850 NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_assertion wasDerivedFrom befree-20140225 NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_assertion wasGeneratedBy ECO_0000203 NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP771713.RAjc_Zq5tAIfJpq3JSju3Oe60nq5hv97yf6FlqUolw1C8130_provenance.