Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_assertion description "[It is a heritable disorder characterised by defective mineralisation of the skeletal and dental structures of the body and a deficiency in the liver/bone/kidney (L/B/K) isoenzyme of alkaline phosphatase (ALP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_assertion evidence source_evidence_literature NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_assertion SIO_000772 8227447 NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_assertion wasDerivedFrom befree-20140225 NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_assertion wasGeneratedBy ECO_0000203 NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP222287.RAxOeK2I6akrn65HfjoPshW6b745qzBFha_5NO5Bgy5Bk130_provenance.