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- source_evidence_literature type ECO_0000212 NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_assertion description "[Identification of seven novel mutations in ABCD1 by a DHPLC-based assay in Italian patients with X-linked adrenoleukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_assertion evidence source_evidence_literature NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_assertion SIO_000772 15643618 NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_assertion wasDerivedFrom befree-2016 NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_assertion wasGeneratedBy ECO_0000203 NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.
- befree-2016 importedOn "2016-02-19" NP475812.RA56dciAFxok54Z7LH_-mPp8fqBXY25MUClxFmXj2Zq68130_provenance.