Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_assertion description "[Methylmalonic aciduria and homocystinuria, cblC type (OMIM 277400), is the most common inborn error of vitamin B(12) (cobalamin) metabolism, with about 250 known cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_assertion evidence source_evidence_literature NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_assertion SIO_000772 16311595 NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_assertion wasDerivedFrom befree-20140225 NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_assertion wasGeneratedBy ECO_0000203 NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.
- befree-20140225 importedOn "2014-02-25" NP392704.RAyfprowduJRp1aO7MwPbZozgLLKmQnkz0FjJw3GKb0Is130_provenance.