Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_assertion description "[Hypophosphatasia is an inherited disorder characterized by defective bone mineralization and deficiency of serum and tissue liver/bone/kidney alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_assertion evidence source_evidence_literature NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_assertion SIO_000772 12815606 NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_assertion wasDerivedFrom befree-20140225 NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_assertion wasGeneratedBy ECO_0000203 NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635163.RA4UvWgkGvlCxzAau4UYDe_PAI2YKZoCAUQv39dnAnLME130_provenance.