Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion> ?p ?o ?g. }
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- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion type Assertion NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_head.
- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion description "[In this study we analyzed the genotype and phenotype of individuals from two unrelated families with HCM in which the affected individuals have the same missense mutation in exon 13 (G1208A) of the coding sequence for beta MHC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_provenance.
- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion evidence source_evidence_literature NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_provenance.
- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion SIO_000772 7934006 NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_provenance.
- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion wasDerivedFrom befree-2016 NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_provenance.
- NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_assertion wasGeneratedBy ECO_0000203 NP1327472.RAyq1QNrn0YEc81pfu6KZHYlXSfrOco061tAhlKXRNxDE130_provenance.