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- source_evidence_literature type ECO_0000212 NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_assertion description "[HRM analysis represents an inexpensive, highly sensitive and high-throughput method to allow identification of mutations in the coding sequences of prevalent HCM genes. Identification of more HCM mutations will provide new insights into genotype/phenotype]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_assertion evidence source_evidence_literature NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_assertion SIO_000772 20800588 NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_assertion wasDerivedFrom gad-20150221 NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_assertion wasGeneratedBy ECO_0000203 NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP184645.RAfbVZU6hO_ai0OQXiMeJ5884jJHNcXngXrnPGANSAA_8130_provenance.