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- source_evidence_literature type ECO_0000212 NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_assertion description "[Therefore, alterations RMRP-S1 and -S2, caused by point mutations in RMRP, are strongly implicated in the molecular mechanism of CHH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_assertion evidence source_evidence_literature NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_assertion SIO_000772 24009312 NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_assertion wasDerivedFrom befree-20150227 NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_assertion wasGeneratedBy ECO_0000203 NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP672359.RAIXjoXk69gD4KwyCVmc-hwqK2J5gq96dRXiC10ZJfk7o130_provenance.