Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_assertion description "[Recently, a unique translocation between the X chromosome and chromosome 1 or t(X;1) has been described in several reports of renal cell carcinomas (RCCs) diagnosed in children and adolescents that results in PRCC-TFE3 gene fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_assertion evidence source_evidence_literature NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_assertion SIO_000772 16807766 NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_assertion wasDerivedFrom befree-20150227 NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_assertion wasGeneratedBy ECO_0000203 NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP639600.RAbHzGW5D-oCrFtNfL9ql277STSkNBgKI4mekz9U-GV2w130_provenance.