Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion> ?p ?o ?g. }
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- NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion type Assertion NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_head.
- NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion description "[Our study thus implies that the Pro56Ser mutation might lead to ALS by eliminating the native MSP structure, which consequently leads to aggregation and loss of functions under physiological conditions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_provenance.
- NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion evidence source_evidence_literature NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_provenance.
- NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion SIO_000772 20377183 NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_provenance.
- NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion wasDerivedFrom befree-20140225 NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_provenance.
- NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_assertion wasGeneratedBy ECO_0000203 NP600905.RAtwav_PyaHacUQniMmRN7vpEVwFP_xn4sPnIT0VS4sPo130_provenance.