Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_assertion description "[To conclude, PD cases exhibited hyperhomocysteinemia and MTRR 66 A>G and cSHMT 1420 C>T gene variants were shown to modulate PD risk by altering the homocysteine levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_assertion evidence source_evidence_literature NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_assertion SIO_000772 24686188 NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_assertion wasDerivedFrom befree-2016 NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_assertion wasGeneratedBy ECO_0000203 NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1169007.RAy4RsMmV53jofF9mTQ38VYDwcIAcwwdCjQ9XI_rjfNGA130_provenance.