Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP578535.RADoi6cnS0Zi6xmQeILN4mrDbhXFhplBYyMHDv-jwGXoI130_provenance.