Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_assertion description "[In summary, we conclude that the NEFH gene is involved in the pathogenesis of sporadic MND.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_assertion evidence source_evidence_literature NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_assertion SIO_000772 14722583 NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_assertion wasDerivedFrom gad-20150221 NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_assertion wasGeneratedBy ECO_0000203 NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67634.RARMFHLwXubAkcvv2fQs4fOvwGEIYKtb3I7Pd0-iGI6Wk130_provenance.