Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion> ?p ?o ?g. }
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- NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion type Assertion NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_head.
- NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion wasGeneratedBy ECO_0000218 NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_provenance.
- NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion wasDerivedFrom uniprot-20130724 NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_provenance.
- NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion SIO_000772 9359047 NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_provenance.
- NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion evidence source_evidence_curated NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_provenance.
- NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_assertion description "[Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1916.RAKcnfuFJgGNtfbAl-lDWblo_wKRZqhde3LjV9zg6q9ew130_provenance.