Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_assertion wasGeneratedBy ECO_0000203 NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_assertion wasDerivedFrom befree-2016 NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_assertion SIO_000772 23403405 NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_assertion evidence source_evidence_literature NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.
- NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_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." NP1052343.RA0DvZFzHiie6VdT5kLmnUE8QVAaj9f7dlw9bHkohvHXc130_provenance.