Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_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." NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_assertion evidence source_evidence_literature NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_assertion SIO_000772 17095158 NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_assertion wasDerivedFrom befree-20150227 NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_assertion wasGeneratedBy ECO_0000203 NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP880719.RAKkMeE2JOP5qdNP9PO5APvmy2A3AK9fI5ORYMMJ-TcbU130_provenance.