Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_assertion description "[Of the five known human RecQ family members, three (BLM, WRN and RECQ4, which cause Bloom's syndrome, Werner's syndrome and Rothmund-Thomson syndrome respectively) are mutated in distinct clinical disorders associated with cancer predisposition and/or premature aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_assertion evidence source_evidence_literature NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_assertion SIO_000772 16246145 NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_assertion wasDerivedFrom befree-20150227 NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_assertion wasGeneratedBy ECO_0000203 NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP268134.RAscLC0idbzVIslAH1BdTYYNx5Tj4U1HWQOJzqMc3UZMI130_provenance.