Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_assertion description "[To report the results of the GUCY2D gene mutation analysis in a cohort of Chinese patients with cone or cone-rod dystrophies (COD or CORD) and to describe the clinical features observed in patients with molecularly confirmed COD or CORD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_assertion evidence source_evidence_literature NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_assertion SIO_000772 26298565 NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_assertion wasDerivedFrom befree-2016 NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_assertion wasGeneratedBy ECO_0000203 NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1293045.RAi7FM01ClAgrGTrTsqAtNcFFaonhCiIWR9bRJNSvsoZU130_provenance.