Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_assertion description "[We find from a literature review that missense mutations within the FNIII domain of MID1 are associated with a milder presentation of OS than missense mutations elsewhere in MID1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_assertion evidence source_evidence_literature NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_assertion SIO_000772 16378742 NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_assertion wasDerivedFrom befree-20150227 NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_assertion wasGeneratedBy ECO_0000203 NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP567150.RAQseSVhvMdByRNAH8_rtJw8ByRwcm1S_1jJLUYnim0jM130_provenance.