Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_assertion description "[The nucleotide diversity of the ABCA4 coding region, a collective measure of the number and prevalence of polymorphic sites in a region of DNA, was found to be 1.28, a value that is 9 to 400 times greater than that of two other macular disease genes that were examined in a similar fashion (VMD2 and EFEMP1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_assertion evidence source_evidence_literature NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_assertion SIO_000772 11328725 NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_assertion wasDerivedFrom befree-2016 NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_assertion wasGeneratedBy ECO_0000203 NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.
- befree-2016 importedOn "2016-02-19" NP316394.RAmGYuhxoTQDg9RyOqI9KZ0MCG9iG5MzuHE0smfbQlQT8130_provenance.