Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_assertion description "[The incidence of GVHD in matched and unmatched groups was respectively: grade I-IV: 81% and 86% (P = 0.492); II-IV 61% and 57% (P = 0.495); III-IV 23% and 21% (P = 0.608).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_assertion evidence source_evidence_literature NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_assertion SIO_000772 17130788 NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_assertion wasDerivedFrom befree-20140225 NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_assertion wasGeneratedBy ECO_0000203 NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651955.RAWfrk98g_ZWcKtWyExH4aCT0ngJnQ0olG3uYYunWs_4w130_provenance.