Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion description "[While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion evidence source_evidence_literature NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion SIO_000772 19507262 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion wasDerivedFrom befree-20150227 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_assertion wasGeneratedBy ECO_0000203 NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978075.RAFMeuLsJxx5AcxSN85R7Dcwx1Mq0oC74hmiZKQWrNvbA130_provenance.