Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP141635.RAlkn42PfwoOo7m2kujbeSTHz_mQ1eYSJdQN8DqwyCvJc130_provenance.