Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_assertion description "[A cerebellar X-linked human ataxia has recently been found to be caused by a mutation in the calmodulin-binding domain of PMCA3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_assertion evidence source_evidence_literature NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_assertion SIO_000772 23413890 NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_assertion wasDerivedFrom befree-20150227 NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_assertion wasGeneratedBy ECO_0000203 NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP279001.RAljthFTBpzr6970gPe01YvSqsMiSWD1a8eCBc3NZbOVQ130_provenance.