Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion description "[To evaluate whether this CHK2 founder mutation is associated with MM in patients with LFS syndrome, more MM cases from LFS families should be examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion evidence source_evidence_literature NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion SIO_000772 15057041 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion wasDerivedFrom befree-20140225 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_assertion wasGeneratedBy ECO_0000203 NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP474223.RAAF47Peye60HVHZOq2qfdXswdX0bht0cv1yD9WQtRrlU130_provenance.