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- source_evidence_literature type ECO_0000212 NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_assertion description "[Based on these data, we suggest that the intrafamilial phenotypic variability in SMA families is not caused by polymorphic variants or transcription differences within Htra2-beta1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_assertion evidence source_evidence_literature NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_assertion SIO_000772 11153908 NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_assertion wasDerivedFrom befree-20150227 NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_assertion wasGeneratedBy ECO_0000203 NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP890377.RAc9-4ex5yafE31G1mhWseZTjrAosquAU8_oWoO_qV4nY130_provenance.