Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion> ?p ?o ?g. }
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- NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion type Assertion NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_head.
- NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion description "[ferroportin mutations A77D, V162delta, and G490D are associated with a typical pattern of hemochromatosis disease in vivo ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_provenance.
- NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion evidence source_evidence_literature NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_provenance.
- NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion SIO_000772 15692071 NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_provenance.
- NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion wasDerivedFrom lhgdn-20090331 NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_provenance.
- NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_assertion wasGeneratedBy ECO_0000203 NP211203.RAsPRNm4LxOFNCqpJIuat3GVKq6waXRQsIOVt7vquLN5Q130_provenance.