Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_assertion description "[However we can not rule out other genetic variation at the LRRK2 locus may play a role in parkinsonian disorders with amyotrophic lateral sclerosis and may be considered candidates for genetic screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_assertion evidence source_evidence_literature NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_assertion SIO_000772 16865326 NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_assertion wasDerivedFrom befree-20140225 NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_assertion wasGeneratedBy ECO_0000203 NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP724385.RAdLvEv2YO2IFSAygssDt3wROwf4juvLcWPH93X54RzuA130_provenance.