Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion description "[Our results show that mutations in the coding region or 3 untranslated region miRNA recognition elements A and B of LIN28B do not underlie CDGP. Lack of any variation in the coding region of the gene suggests that LIN28B in developmental timing is so crucial that any changes in the conserved protein would probably be lethal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion evidence source_evidence_literature NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion SIO_000772 20350940 NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion wasDerivedFrom gad-20130706 NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_assertion wasGeneratedBy ECO_0000203 NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87999.RAwl3loVu-r0POdoII_CIn5tVB1b_f6vMw6djXJ8h7TJA130_provenance.