Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_assertion description "[Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_assertion evidence source_evidence_literature NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_assertion SIO_000772 19251628 NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_assertion wasDerivedFrom befree-2016 NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_assertion wasGeneratedBy ECO_0000203 NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.
- befree-2016 importedOn "2016-02-19" NP723191.RAv5lH5xaWNMYzm_TD9o2tPYkRn7wOxz6FRJvsgX2Mycw130_provenance.