Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_assertion wasGeneratedBy ECO_0000203 NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_assertion wasDerivedFrom befree-20140225 NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_assertion SIO_000772 15911147 NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_assertion evidence source_evidence_literature NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_assertion description "[In order to define if mutation at these loci is a common cause of clinically defined parkinsonism we typed the SCA-2 and SCA-3 repeats for expansion in a series of 280 patients diagnosed with PD or parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP654457.RAwCPmhw4_cTcCo7hk9LrXKFAw2M9zE4feWolUAVN7wtk130_provenance.