Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_assertion description "[Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_assertion evidence source_evidence_literature NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_assertion SIO_000772 19836009 NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_assertion wasDerivedFrom befree-20140225 NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_assertion wasGeneratedBy ECO_0000203 NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635638.RA8wp2CQPGef7npZqAo6CenbCLz0kLwJhLIRVXRyhPAJc130_provenance.