Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion> ?p ?o ?g. }
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- NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion type Assertion NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_head.
- NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion description "[Many of these mutations involve either missense or deletion mutations located in a region of the proSP-C molecule that has structural homology to the BRI family of proteins linked to inherited degenerative dementias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_provenance.
- NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion evidence source_evidence_literature NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_provenance.
- NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion SIO_000772 15709974 NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_provenance.
- NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion wasDerivedFrom befree-2016 NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_provenance.
- NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_assertion wasGeneratedBy ECO_0000203 NP480809.RAFdcPhGxOH1-Ykrua9Cko7MsT0pwMkjxGPyWHObBpZhg130_provenance.