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- source_evidence_literature type ECO_0000212 NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_assertion description "[This study reports on bioinformatic and moleculardata for the FAM46A gene that may give a wider insight into the putative function of this gene and its pathologic relevance to RP25 and other retinal diseases mapping within the 6q chromosomal interval.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_assertion evidence source_evidence_literature NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_assertion SIO_000772 17803723 NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_assertion wasDerivedFrom befree-2016 NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_assertion wasGeneratedBy ECO_0000203 NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.
- befree-2016 importedOn "2016-02-19" NP628585.RAhI666om9H9pHofPQEXdFKX9-OhCIy5fvqL2yOEn0lQ4130_provenance.