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- source_evidence_literature type ECO_0000212 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_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." NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion evidence source_evidence_literature NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion SIO_000772 20947812 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion wasDerivedFrom befree-20150227 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_assertion wasGeneratedBy ECO_0000203 NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP703716.RA6yxs6C6k-dNeOaBmO04TeAN6ExYE0Y8DpXH7xvHHiFs130_provenance.