Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_assertion description "[Mutations in GLUD1 encoding glutamate dehydrogenase, also cause protein sensitive HH (due to leucine sensitivity).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_assertion evidence source_evidence_literature NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_assertion SIO_000772 22583614 NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_assertion wasDerivedFrom befree-20140225 NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_assertion wasGeneratedBy ECO_0000203 NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625639.RAMzfI__-v3raQuRqa53L0lVpGitzvRVX4JcRQzrHGxQU130_provenance.