Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_assertion description "[Using highly informative microsatellite DNA markers in eight multiplex families, we were able to exclude Stargardt's disease from the vicinity of the CLN1 and CLN3 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_assertion evidence source_evidence_literature NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_assertion SIO_000772 8014971 NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_assertion wasDerivedFrom befree-20140225 NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_assertion wasGeneratedBy ECO_0000203 NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP619581.RA46a2yDmELmQM6F3WU8rdWENrcqzXqq4o2Zme7j47Nvc130_provenance.