Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_assertion> ?p ?o ?g. }
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- NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_assertion type Assertion NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_head.
- NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_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." NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_provenance.
- NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_assertion evidence source_evidence_literature NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_provenance.
- NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_assertion SIO_000772 20377183 NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_provenance.
- NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_assertion wasDerivedFrom befree-20150227 NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_provenance.
- NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_assertion wasGeneratedBy ECO_0000203 NP817948.RAIQV-sSnt8dRPbkzAtGhaNI5IA3oEVOn3CQaPuq6RcJw130_provenance.