Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion> ?p ?o ?g. }
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- NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion type Assertion NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_head.
- NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion description "[Clinical findings are different in 9q deletions and duplications including PTCH1, notably concerning the predisposition to benign and malignant tumors reported in the Gorlin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion evidence source_evidence_literature NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion SIO_000772 24486987 NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion wasDerivedFrom befree-20150227 NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_assertion wasGeneratedBy ECO_0000203 NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.