Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_assertion description "[X-linked hypophosphatemia (XLH) is phenotypically similar to OHO and results from mutations in PHEX, a putative metallopeptidase believed to process a factor(s) regulating bone mineralization and renal phosphate reabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_assertion evidence source_evidence_literature NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_assertion SIO_000772 11414762 NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_assertion wasDerivedFrom befree-20140225 NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_assertion wasGeneratedBy ECO_0000203 NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP698130.RAGB0lfopWkov0Idi9Bc5GJCHprRu9L6FilOJjCQG217E130_provenance.