Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_assertion description "[Cases with familial monosomy 7 are well recognized, but there are no reports of familial MDS with deletion of 5q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_assertion evidence source_evidence_literature NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_assertion SIO_000772 8217806 NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_assertion wasDerivedFrom befree-2016 NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_assertion wasGeneratedBy ECO_0000203 NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1335924.RAZoHXFXFa1taUOZQn6gaS1Jr55QgA9HgveJTv94OPdzw130_provenance.