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- NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_assertion type Assertion NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_head.
- NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_assertion wasGeneratedBy ECO_0000203 NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_provenance.
- NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_assertion wasDerivedFrom befree-2016 NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_provenance.
- NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_assertion SIO_000772 23403405 NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_provenance.
- NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_assertion evidence source_evidence_literature NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_provenance.
- NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_assertion description "[These discoveries indicate that ADHR, XLH, and ARHR represent three related heritable hypophosphatemic diseases that arise from mutations in, or dysregulation of, a single common gene product, FGF23 and, in ARHR and XLH, complimentary DMP1 and PHEX directed events that contribute to abnormal bone mineralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1052341.RABlVVVdTbDoqxw8QdpY78PHoop27fVa_S7IvouaRaSOY130_provenance.