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- source_evidence_literature type ECO_0000212 NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_assertion description "[X-linked PNH caused by FLN1 mutations (MIM #300049) implies prenatal or early postnatal lethality in boys and 50% recurrence risk in daughters of affected women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_assertion evidence source_evidence_literature NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_assertion SIO_000772 15249610 NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_assertion wasDerivedFrom befree-20150227 NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_assertion wasGeneratedBy ECO_0000203 NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP406957.RAkhuusad28X9ySLnRt1jtF8q41O2MheJa6BP0z_zXeSE130_provenance.