Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_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." NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_assertion evidence source_evidence_literature NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_assertion SIO_000772 8217806 NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_assertion wasDerivedFrom befree-20150227 NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_assertion wasGeneratedBy ECO_0000203 NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781422.RAWgTw0t8x4d_hybIw8N2PBoic9k7OxlHB8XRX-5h7s50130_provenance.