Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_assertion description "[Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_assertion evidence source_evidence_literature NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_assertion SIO_000772 24676022 NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_assertion wasDerivedFrom befree-20150227 NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_assertion wasGeneratedBy ECO_0000203 NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221996.RAHy-cxX58e6vnVQt4Ao5rU6FerbHNnKFX4RTWlbuNwy4130_provenance.