Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_assertion description "[A preproparathyroid hormone allele from a patient with familial isolated hypoparathyroidism was shown to have a single point mutation in the hydrophobic core of the signal sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_assertion evidence source_evidence_literature NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_assertion SIO_000772 7829495 NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_assertion wasDerivedFrom befree-20140225 NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_assertion wasGeneratedBy ECO_0000203 NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP843248.RAyHZTCvTDezMA5nk023NeXPo9gox2t-lW1mZJZ2xGXVo130_provenance.