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- source_evidence_literature type ECO_0000212 NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_assertion description "[These results imply distinct molecular mechanisms for monosomy 7 and trisomy 8 MDS and implicate specific pathogenic pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_assertion evidence source_evidence_literature NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_assertion SIO_000772 15315976 NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_assertion wasDerivedFrom befree-20150227 NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_assertion wasGeneratedBy ECO_0000203 NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781426.RAEFqS-wSM-6Wvoq1zRarNR0MkKzRWg5bHrdp9o1NNFHo130_provenance.