Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion> ?p ?o ?g. }
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- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion type Assertion NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_head.
- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_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." NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_provenance.
- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion evidence source_evidence_literature NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_provenance.
- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion SIO_000772 20800588 NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_provenance.
- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion wasDerivedFrom gad-20150221 NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_provenance.
- NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_assertion wasGeneratedBy ECO_0000203 NP121317.RAxohLz6TmLq5il9Q20guuDRcOJrCCIcHBDdKq6fHpAJg130_provenance.