Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_assertion> ?p ?o ?g. }
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- NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_assertion type Assertion NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_head.
- NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_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." NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_provenance.
- NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_assertion evidence source_evidence_literature NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_provenance.
- NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_assertion SIO_000772 20377183 NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_provenance.
- NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_assertion wasDerivedFrom befree-20140225 NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_provenance.
- NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_assertion wasGeneratedBy ECO_0000203 NP348766.RAVQmMD30KQsJ050th4NrrJYJXmSK6eHa_IBMBIVlNoS4130_provenance.