Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_assertion description "[LGMD2B mutational analysis in Miyoshi myopathy, and atypical dysferlinopathies ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_assertion evidence source_evidence_literature NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_assertion SIO_000772 16010686 NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_assertion wasDerivedFrom lhgdn-20090331 NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_assertion wasGeneratedBy ECO_0000203 NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP211911.RAO4er0DsPfQ1yOcvB-nxlXnyYcxlmjzfEdjyNiWUH7ew130_provenance.