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- source_evidence_literature type ECO_0000212 NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_assertion evidence source_evidence_literature NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_assertion SIO_000772 18195150 NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_assertion wasDerivedFrom befree-20150227 NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_assertion wasGeneratedBy ECO_0000203 NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP863369.RA1wkm770I41U1pP4SgS_P3X6j5GYMwpstDD4nttQr8p0130_provenance.