Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_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." NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_assertion evidence source_evidence_literature NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_assertion SIO_000772 19251628 NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_assertion wasDerivedFrom befree-20150227 NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_assertion wasGeneratedBy ECO_0000203 NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP414348.RAj1fgU72KuNci-PXMmgVV4BJrWZuY2WO7STr1hl9a4_0130_provenance.