Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion type Assertion NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_head.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion description "[We report here on a case of occlusive stroke at young age and hyperhomocysteinemia with homozygous VN (677C to T) variant in the MTHFR gene as well as homozygous D/D (2756G to A) variant in the MS gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_provenance.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion evidence source_evidence_literature NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_provenance.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion SIO_000772 11460881 NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_provenance.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion wasDerivedFrom befree-2016 NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_provenance.
- NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_assertion wasGeneratedBy ECO_0000203 NP324307.RAKrlWg7eoFnNfb4qpX9PYVnAcouXAY7FsAo8Ama2xFK0130_provenance.