Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion> ?p ?o ?g. }
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- NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion type Assertion NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_head.
- NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion description "[One of the 220 patients (0.45%) with diabetes was homozygous for the HFE 845A (C282Y) mutation and 25 (11.3%) were heterozygous for the same mutation, of whom 3 (1.3%) were compound heterozygotes also carrying the HFE 187G (H63D) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_provenance.
- NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion evidence source_evidence_literature NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_provenance.
- NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion SIO_000772 10695662 NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_provenance.
- NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion wasDerivedFrom befree-20150227 NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_provenance.
- NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_assertion wasGeneratedBy ECO_0000203 NP446788.RANC7lN5_e7qYSR5YuztU8zBMWZHfYwMXRy4mju4vSo4Y130_provenance.