Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_assertion description "[The Pro56Ser mutation in the human VAPB MSP domain causes a familial amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_assertion evidence source_evidence_literature NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_assertion SIO_000772 20377183 NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_assertion wasDerivedFrom befree-20140225 NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_assertion wasGeneratedBy ECO_0000203 NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP432541.RAuXMiObC6r0VTcvOf5xF4uyXqwEmdH4RoggpnKprIluk130_provenance.