Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion> ?p ?o ?g. }
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- NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion type Assertion NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_head.
- NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion wasGeneratedBy ECO_0000203 NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_provenance.
- NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion wasDerivedFrom befree-2016 NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_provenance.
- NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion SIO_000772 17992582 NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_provenance.
- NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion evidence source_evidence_literature NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_provenance.
- NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_assertion description "[This knowledge should help clinicians and basic scientists seize on the opportunity to develop more sensitive and specific screening and management programs in this disease; while a relatively small subset of pancreatic cancer may be readily identifiable through its FAMMM phenotype, coupled with its CDKN2A mutation, this hereditary disorder, given a keen knowledge of its natural history and molecular genetics, may prove to be an effective clinical preventive model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639624.RAPDPojC3stbSpKbKM_gPwXGnrr_YL-lg_8zkdMtXgvrE130_provenance.