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- NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_assertion type Assertion NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_head.
- NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_assertion wasGeneratedBy ECO_0000203 NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_provenance.
- NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_assertion wasDerivedFrom gad-20150221 NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_provenance.
- NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_assertion SIO_000772 10520044 NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_provenance.
- NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_assertion evidence source_evidence_literature NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_provenance.
- NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_assertion description "[Factor V Leiden and the common haemochromatosis mutation HFE C282Y: is there an association in familial venous thromboembolic disease?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50180.RAD6U2JhmmDoH57vnNQRefII56RXml_mizdCmxD22aVS4130_provenance.