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- source_evidence_literature type ECO_0000212 NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_assertion description "[Our results suggest that the A2M deletion polymorphism may not be a definitive risk factor of CAA in the elderly, although further study with larger samples is necessary to confirm this.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_assertion evidence source_evidence_literature NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_assertion SIO_000772 10548657 NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_assertion wasDerivedFrom befree-2016 NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_assertion wasGeneratedBy ECO_0000203 NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.
- befree-2016 importedOn "2016-02-19" NP266891.RAb2LaR6ru_ic44uA9Zvw16MrMzp9ewKMO81unxut1qns130_provenance.