Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_assertion description "[NKX2.5 mutations occur in a small percentage of patients with various congenital heart diseases/. 5 mutations in non-homeodomain regions may be important in the development of human structural cardiac defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_assertion evidence source_evidence_literature NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_assertion SIO_000772 14607454 NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_assertion wasDerivedFrom lhgdn-20090331 NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_assertion wasGeneratedBy ECO_0000203 NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP122166.RAEGRh8wYN3l0w1LJ6cji9ebTWFRK6YmbiMJdQaOb2fH0130_provenance.