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- source_evidence_literature type ECO_0000212 NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_assertion description "[New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_assertion evidence source_evidence_literature NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_assertion SIO_000772 19034539 NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_assertion wasDerivedFrom befree-20150227 NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_assertion wasGeneratedBy ECO_0000203 NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP940653.RAgeMrVOqzpvf5L6FjXsw05Ksvw4lyP_e3iVFD-Dd7cfI130_provenance.