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- source_evidence_literature type ECO_0000212 NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_assertion description "[Polymorphisms in the LOXL1 gene confer risk to XFS/XFG in the Japanese, but there are different risk-associated alleles and haplotypes in the Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_assertion evidence source_evidence_literature NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_assertion SIO_000772 18450598 NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_assertion wasDerivedFrom befree-2016 NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_assertion wasGeneratedBy ECO_0000203 NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.
- befree-2016 importedOn "2016-02-19" NP668841.RAWzqDC3PlEO8uY9ACSpthc6aWKoZ7GzxJo-KE_zi8ltA130_provenance.