Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_assertion description "[She and her 37-year-old brother show the same clinical features such as bowing of legs together with hypophosphatemia (sister: P 1.8 mg/dl, brother: P 1.6 mg/dl) and high FGF23 levels (sister: 542 pg/ml, brother: 96 pg/ml).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_assertion evidence source_evidence_literature NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_assertion SIO_000772 19581284 NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_assertion wasDerivedFrom befree-20150227 NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_assertion wasGeneratedBy ECO_0000203 NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789561.RAvHuNqa1oRI51CUh32srWBo5FIXsTaaYLuDZeXNkFp1c130_provenance.