Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion description "[Hypophosphatasia is a rare inherited disorder characterized by defective bone mineralization and deficiency of serum and liver/bone/kidney-type alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion evidence source_evidence_literature NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion SIO_000772 10679946 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion wasDerivedFrom befree-2016 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_assertion wasGeneratedBy ECO_0000203 NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.
- befree-2016 importedOn "2016-02-19" NP275503.RA88dlVwzcIkB9jMaiNKq-PSPiO_YWjrXA9hJW1GivPTE130_provenance.