Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_assertion description "[Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_assertion evidence source_evidence_literature NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_assertion SIO_000772 10655546 NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_assertion wasDerivedFrom befree-2016 NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_assertion wasGeneratedBy ECO_0000203 NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.
- befree-2016 importedOn "2016-02-19" NP273849.RAsFY8f_DYwxBq7SF4zNLFfGPmjDwOn94JRXAwOKJ-Bps130_provenance.