Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_assertion description "[the identified mutations could contribute to the development of the ASD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_assertion evidence source_evidence_literature NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_assertion SIO_000772 16754686 NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_assertion wasDerivedFrom gad-20150221 NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_assertion wasGeneratedBy ECO_0000203 NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100941.RAmK4EOaf0auZFATWb9PUgl4S8vwkqgONVZswtV0FHmpc130_provenance.