Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_assertion description "[Mutations in genes encoding myosin VIIa, harmonin, cadherin 23, protocadherin 15 or sans cause Usher syndrome type I (USH1, characterized by congenital deafness, vestibular dysfunction and retinitis pigmentosa leading to blindness) in humans and hair bundle disorganization in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_assertion evidence source_evidence_literature NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_assertion SIO_000772 18339676 NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_assertion wasDerivedFrom befree-20140225 NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_assertion wasGeneratedBy ECO_0000203 NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP560637.RAAB8YvbgpwauQG15_FlU_o0ZwpbRt7LINs8qiPqrSvHo130_provenance.