Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_assertion wasGeneratedBy ECO_0000203 NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_assertion wasDerivedFrom befree-2016 NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_assertion SIO_000772 24922459 NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_assertion evidence source_evidence_literature NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.
- NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_assertion description "[Although vascular Ehlers-Danlos syndrome appears to be genetically homogeneous, allelic heterogeneity is marked, and the natural history varies with gender and type of mutation in COL3A1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1191353.RAnlNsRuLEZC4OVx7b62NpZ-c5qIS4nO8_QAHqir5mee4130_provenance.