Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_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." NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_assertion evidence source_evidence_literature NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_assertion SIO_000772 15315976 NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_assertion wasDerivedFrom befree-20150227 NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_assertion wasGeneratedBy ECO_0000203 NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781546.RAxvNsVE6Vu5XzoG2Vq_jSzOA_9TWSbiFMB1hHiLo88GA130_provenance.