Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion> ?p ?o ?g. }
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- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion type Assertion NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_head.
- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion description "[This autosomal dominant inherited disorder is caused by mutations in the gene LEMD3 on chromosome 12q14, which induces a rather heterogeneous clinical phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_provenance.
- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion evidence source_evidence_literature NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_provenance.
- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion SIO_000772 20732851 NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_provenance.
- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion wasDerivedFrom befree-20140225 NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_provenance.
- NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_assertion wasGeneratedBy ECO_0000203 NP615144.RAxV7CybVAH2Ts8hn2peBJloeslP2LQo3wyFQG0umLcUA130_provenance.