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- source_evidence_literature type ECO_0000212 NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_assertion evidence source_evidence_literature NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_assertion SIO_000772 12970307 NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_assertion wasDerivedFrom befree-2016 NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_assertion wasGeneratedBy ECO_0000203 NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.
- befree-2016 importedOn "2016-02-19" NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.