Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_assertion description "[These findings suggest that the neonatal case of hypophosphatasia was associated with compound mutations, one of which caused the loss of ALP activity and the other of which caused a slight reduction of the ALP activity, with a relatively low level of messenger RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_assertion evidence source_evidence_literature NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_assertion SIO_000772 8954059 NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_assertion wasDerivedFrom befree-20140225 NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_assertion wasGeneratedBy ECO_0000203 NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP574321.RAH08UMejBNyYJmyN9CcqmSG_Y0kUS3tDgxaEBqHoocaQ130_provenance.