Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_assertion description "[SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_assertion evidence source_evidence_literature NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_assertion SIO_000772 22972638 NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_assertion wasDerivedFrom befree-20150227 NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_assertion wasGeneratedBy ECO_0000203 NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810230.RA7OeAXHlEi4YmXp0UxFT7VvtIJq0ZvKpoyS4KRePll2I130_provenance.