Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion> ?p ?o ?g. }
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- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion type Assertion NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_head.
- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion description "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_provenance.
- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion evidence source_evidence_literature NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_provenance.
- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion SIO_000772 18800149 NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_provenance.
- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion wasDerivedFrom befree-2016 NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_provenance.
- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion wasGeneratedBy ECO_0000203 NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_provenance.