Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion> ?p ?o ?g. }
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- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion type Assertion NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_head.
- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion description "[Mutations and deletions in the SPG4 gene are responsible for up to 40% of autosomal dominant hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_provenance.
- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion evidence source_evidence_literature NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_provenance.
- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion SIO_000772 17957230 NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_provenance.
- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion wasDerivedFrom befree-20150227 NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_provenance.
- NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_assertion wasGeneratedBy ECO_0000203 NP710054.RAidFv3URkdJ3UEeadwJxldAkyCDkZS1HXJq1ygV6vXqQ130_provenance.