Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_assertion description "[SMN1 and SMN2 exons 7 and 8 differ only by 1 bp each, and SMA diagnosis might be performed by single-strand conformational polymorphism, PCR amplification followed by restriction fragment length polymorphism (RFLP), multiple ligation-dependent probe amplification, or realtime PCR of SMNs exons 7 and 8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_assertion evidence source_evidence_literature NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_assertion SIO_000772 19378506 NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_assertion wasDerivedFrom befree-2016 NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_assertion wasGeneratedBy ECO_0000203 NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.
- befree-2016 importedOn "2016-02-19" NP733332.RA7CmKJtPppZdwDMrokcklK0zSZVrPJsQUZoRtkOas3CY130_provenance.