Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_assertion> ?p ?o ?g. }
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- NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_assertion type Assertion NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_head.
- NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_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." NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_provenance.
- NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_assertion evidence source_evidence_literature NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_provenance.
- NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_assertion SIO_000772 12634862 NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_provenance.
- NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_assertion wasDerivedFrom befree-20150227 NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_provenance.
- NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_assertion wasGeneratedBy ECO_0000203 NP766687.RAYNPfAgOfiqNTjgPbMqcmhdRRLSVVJi28g-GSlA_6b4s130_provenance.