Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_assertion description "[Although SC35, SRp40 and SRp55 proteins all bound to the wild-type and mutated sequences with similar intensities, there was increased binding of ASF/SF2 to the two ADVIRC-mutated sequences compared with the wild-type or Best disease-mutated sequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_assertion evidence source_evidence_literature NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_assertion SIO_000772 18611979 NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_assertion wasDerivedFrom befree-20140225 NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_assertion wasGeneratedBy ECO_0000203 NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889008.RAQvhwuDo758R3St1EK8c1clQ7nVDSIeSu2lzqrO_QTe0130_provenance.