Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_assertion description "[Best's macular dystrophy (BMD), also known as vitelliform macular degeneration type 2 (VMD2; OMIM 153700), is an autosomal dominant form of macular degeneration with mainly juvenile onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_assertion evidence source_evidence_literature NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_assertion SIO_000772 10394929 NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_assertion wasDerivedFrom befree-2016 NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_assertion wasGeneratedBy ECO_0000203 NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.
- befree-2016 importedOn "2016-02-19" NP256646.RARA2LTuAdeNTB7tjcjMWS-JqgwilKheWiRrrYZ9M0Nt0130_provenance.