Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_assertion description "[Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_assertion evidence source_evidence_literature NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_assertion SIO_000772 12121355 NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_assertion wasDerivedFrom befree-2016 NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_assertion wasGeneratedBy ECO_0000203 NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.
- befree-2016 importedOn "2016-02-19" NP361491.RAZkDb4y9xL6GMe7iejrOBH3oeDwmR3uO8AbXBqChYUfM130_provenance.