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- source_evidence_literature type ECO_0000212 NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_assertion description "[We have determined the mutations and the pattern of inheritance of the XPD alleles in the 11 cases identified in Italy so far, in which the hair abnormalities diagnostic for TTD are associated with different disease severity but similar cellular photosensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_assertion evidence source_evidence_literature NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_assertion SIO_000772 9758621 NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_assertion wasDerivedFrom befree-20150227 NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_assertion wasGeneratedBy ECO_0000203 NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381932.RADeXhF_H9Wc7VaTCPfmfTddnRBCinKmB49uwhQLsiiNE130_provenance.