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- source_evidence_literature type ECO_0000212 NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_assertion description "[We clarify the range of NPHS1 mutations in CNF, detecting mutation 'hot-spots' within the NPHS1 coding sequence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_assertion evidence source_evidence_literature NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_assertion SIO_000772 11854170 NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_assertion wasDerivedFrom befree-20150227 NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_assertion wasGeneratedBy ECO_0000203 NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP597408.RAkMIwkfPQWL_M1GfXLVjAOsvSjUkUoFs9jFfVGVPvaKA130_provenance.