Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_assertion description "[Mutations in seven genes cause FTD, with those in tau (MAPT), chromosome 9 open reading frame 72 (C9ORF72), and progranulin (GRN) being the most common.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_assertion evidence source_evidence_literature NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_assertion SIO_000772 22355793 NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_assertion wasDerivedFrom befree-2016 NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_assertion wasGeneratedBy ECO_0000203 NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.
- befree-2016 importedOn "2016-02-19" NP962641.RAj44gXKSllzR3zMjDQrTqDG7CMNLW6wDYj-DLZRrNxLA130_provenance.