Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_assertion description "[Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_assertion evidence source_evidence_literature NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_assertion SIO_000772 21911584 NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_assertion wasDerivedFrom befree-2016 NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_assertion wasGeneratedBy ECO_0000203 NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.
- befree-2016 importedOn "2016-02-19" NP923260.RAT2IpTfmJuTUNUL_I6Vq_gEYQsY0SktfXgGFarfYfkL4130_provenance.