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- source_evidence_literature type ECO_0000212 NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_assertion description "[Hypophosphatasia is an inherited disorder characterized by defective mineralization of the skeletal and dental structures of the body and deficient liver/bone/kidney alkaline phosphatase (L/B/K ALP) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_assertion evidence source_evidence_literature NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_assertion SIO_000772 1432739 NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_assertion wasDerivedFrom befree-20140225 NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_assertion wasGeneratedBy ECO_0000203 NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583216.RA1L-G-gTUs46fo_7CfxMZVwNjdjNfj99735uW7j-1bGw130_provenance.