Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_assertion wasGeneratedBy ECO_0000203 NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_assertion wasDerivedFrom befree-20140225 NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_assertion SIO_000772 16873670 NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_assertion evidence source_evidence_literature NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_assertion description "[LMO2 rearrangements, including this del(11)(p12p13) and t(11;14) (p13;q11) or t(7;11)(q35;p13), were found in the absence of other recurrent cytogenetic abnormalities involving HOX11L2, HOX11, CALM-AF10, TAL1, MLL, or MYC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP724398.RA0N1uXE-fRjniYxDzC9tMppxWjQDH-Txz7qfZ7QdqXE4130_provenance.