Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion> ?p ?o ?g. }
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- NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion type Assertion NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_head.
- NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion description "[The frequency of UBQLN2 and PFN1 genetic variants in the FTLD patients was low at 0.30% and 0.91% respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion evidence source_evidence_literature NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion SIO_000772 23312802 NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion wasDerivedFrom befree-2016 NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_assertion wasGeneratedBy ECO_0000203 NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.