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- source_evidence_literature type ECO_0000212 NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_assertion description "[Because some ARO patients have mutations in both copies of the ClCN7 gene, ADO II is allelic with a subset of ARO cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_assertion evidence source_evidence_literature NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_assertion SIO_000772 11741829 NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_assertion wasDerivedFrom befree-20150227 NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_assertion wasGeneratedBy ECO_0000203 NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP958495.RARt9K0c4-cBJCA86Hke_GUC4XMD_hJfbRX7bM7HHJWZ4130_provenance.