Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_assertion description "[We conclude that ELAC2/HPC2 truncating mutations are rare in HPC, but that rare variants of the ELAC2/HPC2 require additional study as risk factors for PRCA in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_assertion evidence source_evidence_literature NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_assertion SIO_000772 11507049 NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_assertion wasDerivedFrom befree-20150227 NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_assertion wasGeneratedBy ECO_0000203 NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP935933.RAfUm_2wVAeT3FKsLpjs-sFhT1hjeXUTe_-SDsgrDp85Q130_provenance.