Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_assertion description "[An in-frame deletion of 17 amino acids in the second fibronectin type III repeat of integrin beta 4 (delta 17-beta 4) has been associated with junctional epidermolysis bullosa with pyloric atresia (PA-JEB), a genetic disease characterized by altered HD and disadhesion of the epidermis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_assertion evidence source_evidence_literature NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_assertion SIO_000772 9389789 NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_assertion wasDerivedFrom befree-20140225 NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_assertion wasGeneratedBy ECO_0000203 NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP862189.RANXE3MgaptEigNylyBuPX-YgwMXRkrVa47tqHEzq0jkQ130_provenance.