Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_assertion description "[Common MEFV mutations among Jewish ethnic groups in Israel: high frequency of carrier and phenotype IIIstates and absence of a perceptible biological advantage for the carrier state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_assertion evidence source_evidence_literature NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_assertion SIO_000772 11484206 NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_assertion wasDerivedFrom gad-20150221 NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_assertion wasGeneratedBy ECO_0000203 NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP70906.RAWtnqDbfnGrcMEhHvB2T8C-4z4pAJoHJsuSlPFTEw_jA130_provenance.