Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_assertion wasGeneratedBy ECO_0000203 NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_assertion wasDerivedFrom befree-20150227 NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_assertion SIO_000772 1353052 NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_assertion evidence source_evidence_literature NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.
- NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_assertion description "[Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565238.RAB0FE2fysqLldnwLnboQ3BQ_Tb53S1oCLKSsLbJpg2JQ130_provenance.