Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP303092.RAFfx987fF7s8ksOGE14XkSInvsFr0AEY1TmA0PyxDhkI130_provenance.