Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_assertion description "[We report the characterisation of tissue-nonspecific alkaline phosphatase (TNSALP) gene mutations in a series of 13 European families affected by perinatal, infantile or childhood hypophosphatasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_assertion evidence source_evidence_literature NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_assertion SIO_000772 9781036 NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_assertion wasDerivedFrom befree-20150227 NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_assertion wasGeneratedBy ECO_0000203 NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP236876.RAXLwa0G9r-MazuQFm2hwIXUdXntI8G-eBoS0ZS4ei34c130_provenance.