Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion> ?p ?o ?g. }
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- NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion type Assertion NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_head.
- NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion description "[This very low factor IX level and severe bleeding tendency of the patient would be consistent with the homozygous state, but since a double mutation is extremely rare the patient's laboratory findings can be more easily explained by extreme lyonization of the normal X-chromosome of a heterozygous carrier.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_provenance.
- NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion evidence source_evidence_literature NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_provenance.
- NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion SIO_000772 7166026 NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_provenance.
- NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion wasDerivedFrom befree-20140225 NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_provenance.
- NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_assertion wasGeneratedBy ECO_0000203 NP337415.RAMA1PWGLMS-sO9UXMiVnwZmN0tozd8ZyFI7j5v2LdQb4130_provenance.