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- source_evidence_literature type ECO_0000212 NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_assertion description "[ PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined. Our data may facilitate future investigations of patients with various (other) forms of inherited retinal ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_assertion evidence source_evidence_literature NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_assertion SIO_000772 16288196 NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_assertion wasDerivedFrom gad-20150221 NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_assertion wasGeneratedBy ECO_0000203 NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP66817.RAjgxICiyUrOPK3oltB7if0SRhTMBJRCV_tc_-bPyItvo130_provenance.