Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_assertion description "[Because neither galactocerebrosidase activity nor most genotypes reliably predict phenotype, the World Wide Registry was developed to determine whether other clinical/neurodiagnostic data could predict early infantile Krabbe disease in the newborn screening population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_assertion evidence source_evidence_literature NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_assertion SIO_000772 21824559 NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_assertion wasDerivedFrom befree-2016 NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_assertion wasGeneratedBy ECO_0000203 NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.
- befree-2016 importedOn "2016-02-19" NP915482.RA-V8XTQjHvMCLPX0HCQKc0OGzH59eTsSdafz0po7NKJE130_provenance.