Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion> ?p ?o ?g. }
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- NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion type Assertion NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_head.
- NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion description "[Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion evidence source_evidence_literature NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion SIO_000772 17095158 NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion wasDerivedFrom befree-2016 NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_assertion wasGeneratedBy ECO_0000203 NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.