Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_assertion description "[Short-chain acyl-CoA dehydrogenase gene variant, with 625 G-to-A and 511 C-to-T changes, impairs C4-C6 fatty acid metabolism and variably causes neonatal/infantile hypotonia with developmental delays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_assertion evidence source_evidence_literature NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_assertion SIO_000772 18184946 NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_assertion wasDerivedFrom befree-20140225 NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_assertion wasGeneratedBy ECO_0000203 NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP824869.RA_NAR-I7bpqIB0t4uT7349ahjmNQfcTA3vI-3jtmoVkM130_provenance.