Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_assertion description "[First case of L1CAM gene mutation identified in MASA syndrome in Asia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_assertion evidence source_evidence_literature NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_assertion SIO_000772 15904436 NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_assertion wasDerivedFrom befree-20150227 NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_assertion wasGeneratedBy ECO_0000203 NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768578.RAUyh17lQxvXz86-eJ357uabDvoit74oJsC_A_zD4gQ_Q130_provenance.