Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_assertion description "[Recent observations suggest that the human episodic ataxia 2 (EA2) and spinocerebellar ataxia types 6 (SCA6), 12 (SCA12), and 14 (SCA14) might be associated with impaired phosphorylation levels of cerebellum calcium channels and receptors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_assertion evidence source_evidence_literature NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_assertion SIO_000772 19488825 NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_assertion wasDerivedFrom befree-20150227 NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_assertion wasGeneratedBy ECO_0000203 NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP277042.RAWY8ZrqOSKGmJpzAxZ4boFBX1kAo_Nx3IOYJQ2yTredo130_provenance.