Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_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." NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_assertion evidence source_evidence_literature NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_assertion SIO_000772 20947812 NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_assertion wasDerivedFrom befree-20140225 NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_assertion wasGeneratedBy ECO_0000203 NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP291005.RAeR5Xxk6oobOvVN-naVUd6WTDZvg5-c2v06ZPCzK1nv4130_provenance.