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- source_evidence_literature type ECO_0000212 NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_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." NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_assertion evidence source_evidence_literature NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_assertion SIO_000772 10679946 NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_assertion wasDerivedFrom befree-20150227 NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_assertion wasGeneratedBy ECO_0000203 NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881038.RArEM1BLjDe-oTt8D4aIlNzq-TxlyCE-0XkM_ywojZnJw130_provenance.