Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_assertion> ?p ?o ?g. }
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- NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_assertion type Assertion NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_head.
- NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_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." NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_assertion evidence source_evidence_literature NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_assertion SIO_000772 15709974 NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_assertion wasDerivedFrom befree-20140225 NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_assertion wasGeneratedBy ECO_0000203 NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.