Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion> ?p ?o ?g. }
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- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion type Assertion NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_head.
- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion wasGeneratedBy ECO_0000203 NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_provenance.
- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion wasDerivedFrom befree-2016 NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_provenance.
- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion SIO_000772 15695377 NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_provenance.
- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion evidence source_evidence_literature NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_provenance.
- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_provenance.