Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_assertion description "[Silver-Russell syndrome (SRS) is characterized by growth failure and dysmorphic features and is frequently caused by hypomethylation (epimutation) of the H19-DMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_assertion evidence source_evidence_literature NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_assertion SIO_000772 18607558 NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_assertion wasDerivedFrom befree-20150227 NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_assertion wasGeneratedBy ECO_0000203 NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP961026.RAPvMuPgMXlmDw8oNxwhtk0dqNQX32D2YhXbzYL0-r-fs130_provenance.