Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion type Assertion NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_head.
- NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion description "[Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_provenance.
- NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion evidence source_evidence_curated NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_provenance.
- NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion SIO_000772 7981750 NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_provenance.
- NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion wasDerivedFrom uniprot-20130724 NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_provenance.
- NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_assertion wasGeneratedBy ECO_0000218 NP1172.RAiQvV1ihIXbL5Ide-E9vm7UQccpJ9LCoRRtNE3LXQl0o130_provenance.