Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion> ?p ?o ?g. }
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- NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion type Assertion NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_head.
- NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion description "[LRRK2 mutations are a common cause of Parkinson's disease in Spain]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_provenance.
- NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion evidence source_evidence_literature NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_provenance.
- NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion SIO_000772 16643318 NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_provenance.
- NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion wasDerivedFrom gad-20150221 NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_provenance.
- NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_assertion wasGeneratedBy ECO_0000203 NP100300.RAeokfpgr0oAE_m2GmfTXKIg-bPnqlx_UJgZRbGETdHME130_provenance.