Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion description "[In contrast to ALS, the risk of which is influenced by various factors other than SMN copy number itself, the association studies in LMND show a consistent finding that homozygous deletion of SMN2 may be specifically related to LMND, despite the small number of subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion evidence source_evidence_literature NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion SIO_000772 20947812 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion wasDerivedFrom befree-2016 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_assertion wasGeneratedBy ECO_0000203 NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.
- befree-2016 importedOn "2016-02-19" NP845774.RAe7IWlm84yEo1mwgc9NnnapvlSdCjmz1euVMYTPZoAsI130_provenance.