Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_assertion description "[Defects in plectin cause epidermolysis bullosa simplex (EBS), muscular dystrophy (MD), and sometimes pyloric atresia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_assertion evidence source_evidence_literature NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_assertion SIO_000772 21263134 NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_assertion wasDerivedFrom befree-20150227 NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_assertion wasGeneratedBy ECO_0000203 NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP629823.RAQPoHCmO3TGGZAbDeU8Tz4oMooYqSP9XIaQVblyJCTbE130_provenance.