Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_assertion description "[These data indicate that mutations in CLRN1 are associated not only with USH3, but also with nonsyndromic arRP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_assertion evidence source_evidence_literature NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_assertion SIO_000772 21310491 NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_assertion wasDerivedFrom befree-20140225 NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_assertion wasGeneratedBy ECO_0000203 NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP809911.RAKM4s8jW6BsGcyQ6PkdbNjvhhC81lG5pXZcHDCo5BOA4130_provenance.