Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_assertion description "[In another XLRP family, a nonsense mutation (g.ORF15+810G>T) was identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_assertion evidence source_evidence_literature NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_assertion SIO_000772 21683121 NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_assertion wasDerivedFrom befree-2016 NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_assertion wasGeneratedBy ECO_0000203 NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.
- befree-2016 importedOn "2016-02-19" NP902936.RAzv3Zj5gdUSOeRZ91XOLgvHEtl_KVN5n_1djuKSkxbBs130_provenance.