Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_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." NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_assertion evidence source_evidence_literature NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_assertion SIO_000772 8227447 NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_assertion wasDerivedFrom befree-20140225 NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_assertion wasGeneratedBy ECO_0000203 NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP773629.RAM7LMxwzaQZQmy_9RG6u11qlSu1PX8c1dMo7QDgJTvi0130_provenance.