Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_assertion evidence source_evidence_literature NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_assertion SIO_000772 17223983 NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_assertion wasDerivedFrom befree-20140225 NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_assertion wasGeneratedBy ECO_0000203 NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569101.RAaYIGeEm_aMF9eMfAVHtMe1FQ_e5Pmy2lgxa7KABrSmI130_provenance.