Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP653143.RAJrLFP7xNLm99CRcvR-ZpJcmS6fFLJrfOtpvdxU1DrwE130_provenance.