Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion description "[We studied nine Italian families with a pure form of autosomal dominant spastic paraplegia (ADHSP) to assess the frequency of mutations in the SPG4 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion evidence source_evidence_literature NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion SIO_000772 11985387 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion wasDerivedFrom befree-20150227 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_assertion wasGeneratedBy ECO_0000203 NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710063.RAOofpvzPzTh5WHlIl68hRnVyXojeP0BdGweBXEgZq6MM130_provenance.