Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_assertion evidence source_evidence_literature NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_assertion SIO_000772 15639189 NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_assertion wasDerivedFrom befree-2016 NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_assertion wasGeneratedBy ECO_0000203 NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.
- befree-2016 importedOn "2016-02-19" NP475373.RAFaHeiWD9HYAfTmDk2BBSyUD_Fi15P7ASrG2MKvGqJ6U130_provenance.