Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_assertion description "[In three affected individuals in two generations of one family with amyotrophic lateral sclerosis (ALS), a single base-pair change from A to G is found at position 1028 in TDP-43.providing a new insight into the molecular pathogenesis of ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_assertion evidence source_evidence_literature NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_assertion SIO_000772 18438952 NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_assertion wasDerivedFrom lhgdn-20090331 NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_assertion wasGeneratedBy ECO_0000203 NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP140614.RAfvJwImBv3mTo8v3UAEnJnO4XE1F0U7ALoc7_BjYCScg130_provenance.