Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- befree-2016 importedOn "2016-02-19" NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_assertion wasGeneratedBy ECO_0000203 NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_assertion wasDerivedFrom befree-2016 NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_assertion SIO_000772 19762329 NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_assertion evidence source_evidence_literature NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.
- NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_assertion description "[However, in this study, a general role of HMGA2 mutations for SRS was excluded by sequencing of 20 idiopathic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP763936.RALO4uWmejmqQxeG3VtpdNcYWWQDkBKgLthqfianuVDiU130_provenance.