Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion type Assertion NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_head.
- NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion description "[Clinically, POLG mutations can present from early neonatal life to late middle age, with a spectrum of phenotypes that includes common neurological disorders such as migraine, epilepsy and Parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_provenance.
- NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion evidence source_evidence_literature NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_provenance.
- NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion SIO_000772 16987890 NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_provenance.
- NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion wasDerivedFrom befree-20140225 NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_provenance.
- NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_assertion wasGeneratedBy ECO_0000203 NP831473.RAwuB_V9I6bjLOiVixjY8Te0U_31BPu0PS78_J9v5GviQ130_provenance.