Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_assertion description "[BBS2 is a clinically and genetically heterogeneous group of disorders resulting in rod-cone dystrophy, obesity, postaxial polydactyly, renal dysfunction, and mental retardation, which were very recently associated with a novel gene designated BBS2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_assertion evidence source_evidence_literature NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_assertion SIO_000772 11707781 NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_assertion wasDerivedFrom befree-2016 NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_assertion wasGeneratedBy ECO_0000203 NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.
- befree-2016 importedOn "2016-02-19" NP336371.RA6QIk1b4eKopznPXBoCt0AFckrCijavPKhEzUw1QzZ1c130_provenance.