Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_assertion description "[Mutations in the RDS gene, which encodes the photoreceptor glycoprotein peripherin, have been sought in families with autosomal dominant retinal dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_assertion evidence source_evidence_literature NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_assertion SIO_000772 8485576 NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_assertion wasDerivedFrom befree-20150227 NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_assertion wasGeneratedBy ECO_0000203 NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP649250.RALbATZIqN8pxmRM4KG-BbywzDciwvpzayBeMFjB2vwF0130_provenance.