Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion> ?p ?o ?g. }
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- NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion type Assertion NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_head.
- NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion description "[identification of six novel point mutations and one large intragenic deletion in hereditary spastic paraplegia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion evidence source_evidence_literature NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion SIO_000772 18200586 NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion wasDerivedFrom lhgdn-20090331 NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_assertion wasGeneratedBy ECO_0000203 NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.