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- source_evidence_literature type ECO_0000212 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion evidence source_evidence_literature NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion SIO_000772 16453125 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion wasDerivedFrom befree-2016 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_assertion wasGeneratedBy ECO_0000203 NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.
- befree-2016 importedOn "2016-02-19" NP534198.RAwmhpxKR-1olJc7IjAZ61DBNWVl4TvwttHt1Y65rSEHU130_provenance.