Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_assertion description "[Recent studies in four kindreds showed linkage of a gene for FJHN to the same genomic interval on chromosome 16p11.2, where the gene for the phenotypically similar medullary cystic disease type 2 (MCKD2) has been localised.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_assertion evidence source_evidence_literature NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_assertion SIO_000772 12634862 NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_assertion wasDerivedFrom befree-20140225 NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_assertion wasGeneratedBy ECO_0000203 NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP531196.RAOwYseusN5M_RC9g-3QBmxZ-oUyBn7d7OFCQpojwEeZ8130_provenance.