Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_assertion description "[Patients in whom no mutation is identified through this mutation protocol, may be sub-cohorts representing a different FAP pathogenesis including MYH associated polyposis and somatic cell mosaicism for APC gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_assertion evidence source_evidence_literature NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_assertion SIO_000772 19414146 NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_assertion wasDerivedFrom befree-20150227 NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_assertion wasGeneratedBy ECO_0000203 NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP648713.RAXJ1HAkF0XfKB3s5Qp50qfVuYdBZ0810rhxK7PxeIVfE130_provenance.