Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion> ?p ?o ?g. }
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- NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion type Assertion NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_head.
- NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion description "[Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_provenance.
- NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion evidence source_evidence_literature NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_provenance.
- NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion SIO_000772 20215591 NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_provenance.
- NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion wasDerivedFrom befree-20140225 NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_provenance.
- NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_assertion wasGeneratedBy ECO_0000203 NP770131.RAPOaO995DwveiqbUKHFa2pHCPL9Ox5t2HETF_uJxxeKI130_provenance.