Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- befree-2016 importedOn "2016-02-19" NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_assertion wasGeneratedBy ECO_0000203 NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_assertion wasDerivedFrom befree-2016 NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_assertion SIO_000772 21293852 NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_assertion evidence source_evidence_literature NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.
- NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_assertion description "[Three novel mutations in the PHEX gene in Chinese subjects with hypophosphatemic rickets extends genotypic variability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870178.RAulCzzfp1FpNqwvHx_Q4ba-pNHNlcAj5lOV9G2HDr9fE130_provenance.