Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_assertion description "[We also revealed that mutations in RLBP1 may lead to FAP with cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_assertion evidence source_evidence_literature NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_assertion SIO_000772 22559933 NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_assertion wasDerivedFrom befree-20150227 NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_assertion wasGeneratedBy ECO_0000203 NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP672253.RAWpZdq6gCIz947CVT8E4AfDmR6l3SxQEr7PyWk4nQ3J4130_provenance.