Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion type Assertion NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_head.
- NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion wasGeneratedBy ECO_0000203 NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_provenance.
- NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion wasDerivedFrom befree-2016 NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_provenance.
- NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion SIO_000772 18184292 NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_provenance.
- NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion evidence source_evidence_literature NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_provenance.
- NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_assertion description "[We propose that D999H is a novel FHM ATP1A2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649149.RA9urF2EFRD0EStOQlfKuLQlxBYqc7wm-ba1TTCOk-NJo130_provenance.