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- source_evidence_literature type ECO_0000212 NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_assertion description "[A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_assertion evidence source_evidence_literature NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_assertion SIO_000772 9559983 NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_assertion wasDerivedFrom befree-2016 NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_assertion wasGeneratedBy ECO_0000203 NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1393757.RAqDMgDnc66mamGH-XtSwCw2gwyN1S1Hpd-iw_VpglZKw130_provenance.