Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion> ?p ?o ?g. }
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- NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion type Assertion NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_head.
- NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion description "[The X-linked form of CGD, representing approximately 70% of all cases, is caused by mutations in the cytochrome b beta subunit (CYBB) gene, which maps to chromosome Xp21.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_provenance.
- NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion evidence source_evidence_literature NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_provenance.
- NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion SIO_000772 15858141 NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_provenance.
- NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion wasDerivedFrom befree-2016 NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_provenance.
- NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_assertion wasGeneratedBy ECO_0000203 NP491935.RAACJhQqHoRLPB3s9F_xZznTP_bQ9qTEOnYGiSOJloV8g130_provenance.