Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion type Assertion NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_head.
- NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion description "[Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_provenance.
- NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion evidence source_evidence_curated NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_provenance.
- NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion SIO_000772 11438991 NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_provenance.
- NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion wasDerivedFrom uniprot-2016 NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_provenance.
- NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_assertion wasGeneratedBy ECO_0000218 NP1497.RADwH-wZpTkhVsqMjHzXL1bEQD1XqhyGOk4PQ_22tECY0130_provenance.