Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_assertion description "[Mutations in the MYO7A gene cause a deaf-blindness disorder, known as Usher syndrome 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_assertion evidence source_evidence_literature NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_assertion SIO_000772 21493626 NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_assertion wasDerivedFrom befree-2016 NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_assertion wasGeneratedBy ECO_0000203 NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.
- befree-2016 importedOn "2016-02-19" NP887068.RA64qk5Yj3oEXF6mc4Y_OHNkbFrsoXm5ThB3YYjSTTRmc130_provenance.