Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_assertion description "[Clonal patterns were found in 3 of 10 cases of syncytial variant of NSHD, including 2 of 3 (67%) CD20+ cases and 1 of 7 (14%) B-cell antigen-negative cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_assertion evidence source_evidence_literature NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_assertion SIO_000772 7572792 NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_assertion wasDerivedFrom befree-20140225 NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_assertion wasGeneratedBy ECO_0000203 NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP854206.RAlKT0p8J4z7iaYoEYMyAcRQvCjIVDzGc3aMQEmnKIpbc130_provenance.