Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_assertion description "[Molecular heterogeneity of the NUP98/HOXA9 fusion transcript in myelodysplastic syndromes associated with t(7;11)(p15;p15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_assertion evidence source_evidence_literature NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_assertion SIO_000772 10583265 NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_assertion wasDerivedFrom befree-20150227 NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_assertion wasGeneratedBy ECO_0000203 NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP462505.RAaj7J8tyI0VnkUnjn4sDI9bCoI1hI8LbqK_6LObRCdyw130_provenance.