Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_assertion wasGeneratedBy ECO_0000203 NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_assertion wasDerivedFrom befree-20140225 NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_assertion SIO_000772 23403405 NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_assertion evidence source_evidence_literature NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_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." NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP199181.RAs4qmcmm_TR8Gr-S_MSsZEPLv5z2W0NHiI1xZDCk0Nh4130_provenance.