Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_assertion description "[Mutations in the MYO7A gene cause a deaf-blindness disorder, known as Usher syndrome 1B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_assertion evidence source_evidence_literature NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_assertion SIO_000772 21493626 NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_assertion wasDerivedFrom befree-20140225 NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_assertion wasGeneratedBy ECO_0000203 NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.
- befree-20140225 importedOn "2014-02-25" NP516965.RABWSKNbCifeBTk9FDVBB1GLc__Gbmkbav6c1-49nvago130_provenance.