Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_assertion description "[Our findings suggest that abnormalities of the RB-1 gene and its expression are rare in MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_assertion evidence source_evidence_literature NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_assertion SIO_000772 8528059 NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_assertion wasDerivedFrom befree-20150227 NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_assertion wasGeneratedBy ECO_0000203 NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.
- befree-20150227 importedOn "2015-02-27" NP666930.RApT6wwl7b_k8WvCRDb41K3XcgO3JPK1gFmTLckrZK3co130_provenance.