Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_assertion type Assertion NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_head.
- NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_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." NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_provenance.
- NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_assertion evidence source_evidence_literature NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_provenance.
- NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_assertion SIO_000772 16987890 NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_provenance.
- NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_assertion wasDerivedFrom befree-20150227 NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_provenance.
- NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_assertion wasGeneratedBy ECO_0000203 NP633476.RA6TCS4UUIPaE-lC7cpaQcwN4h5TXzX5no7vOKaprg708130_provenance.