Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1042985.RAZciI4uM2q9hlN6BzfsxRTruyzoU0s5Zwar30nGShcJw130_provenance.