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- source_evidence_literature type ECO_0000212 NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_assertion description "[FVL gene mutation was evaluated in patients with severe pregnancy complications in northern Finland/mutation was heterozygous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_assertion evidence source_evidence_literature NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_assertion SIO_000772 16514238 NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_assertion wasDerivedFrom lhgdn-20090331 NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_assertion wasGeneratedBy ECO_0000203 NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215893.RAi7SQQL9EuVhtdp1lX9nYk_Gz59SK7cMgG9ghLHKraVA130_provenance.