Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_assertion description "[found abnormal expression of both PMCA and SERCA-type CA2+-ATPases in platelets of patients with adolescent idiopathic scoliosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_assertion evidence source_evidence_literature NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_assertion SIO_000772 16973504 NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_assertion wasDerivedFrom lhgdn-20090331 NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_assertion wasGeneratedBy ECO_0000203 NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP207455.RAexP9zh0d7TNXArzyW6mPLt4B046090nvHr1Rh_eXhTM130_provenance.