Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_assertion description "[Using the Universal Mutation Database (UMD) software, we have constructed 'UMD-USHbases', a set of relational databases of nucleotide variations for seven genes involved in Usher syndrome (MYO7A, CDH23, PCDH15, USH1C, USH1G, USH3A and USH2A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_assertion evidence source_evidence_literature NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_assertion SIO_000772 18484607 NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_assertion wasDerivedFrom befree-20150227 NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_assertion wasGeneratedBy ECO_0000203 NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP584116.RABkGMIgtuDHKdvxelbJ38mGWJ2Lacu-YXdDP7vMHmGNw130_provenance.