Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_assertion description "[We also recommend that the gene symbols CSNB1 and CSNB2 be used for complete congenital stationary night blindness and Aland disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_assertion evidence source_evidence_literature NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_assertion SIO_000772 2667510 NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_assertion wasDerivedFrom befree-20140225 NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_assertion wasGeneratedBy ECO_0000203 NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP512900.RA9YX4ZGeIgi5sKr94yQXOtNkzxhRDevcZw_OxKE24ww8130_provenance.