Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion type Assertion NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_head.
- NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion wasGeneratedBy ECO_0000218 NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_provenance.
- NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion wasDerivedFrom uniprot-20130724 NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_provenance.
- NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion SIO_000772 14985400 NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_provenance.
- NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion evidence source_evidence_curated NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_provenance.
- NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_assertion description "[A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3806.RAW_CKDuWtuhSkM_uFinwgMBXAAmf9nHkUQ8ByshRgBAw130_provenance.