Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_assertion description "[Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_assertion evidence source_evidence_literature NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_assertion SIO_000772 11231903 NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_assertion wasDerivedFrom befree-20150227 NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_assertion wasGeneratedBy ECO_0000203 NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.
- befree-20150227 importedOn "2015-02-27" NP895172.RANFOfZFxq0Xr7Nlhc6mmNeR2gehZHyPoR8ALoVNWCEac130_provenance.