Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_assertion description "[To test directly the effect of this mutation on FANCA function, we used retroviral-mediated transduction to express either wild-type FANCA or FANCA(H1110P) protein in the FA-A fibroblast line, GM6914.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_assertion evidence source_evidence_literature NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_assertion SIO_000772 10210316 NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_assertion wasDerivedFrom befree-2016 NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_assertion wasGeneratedBy ECO_0000203 NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.
- befree-2016 importedOn "2016-02-19" NP250677.RAx_EL8KvoEqhlFJrFI7JOUjVnQYkooPNXxzXDFut-Spo130_provenance.