Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_assertion description "[Recent studies have identified mutations that cause lipin-1 or lipin-2 deficiency in humans, leading to acute myoglobinuria in childhood or the inflammatory disorder Majeed syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_assertion evidence source_evidence_literature NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_assertion SIO_000772 19369868 NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_assertion wasDerivedFrom befree-2016 NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_assertion wasGeneratedBy ECO_0000203 NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.
- befree-2016 importedOn "2016-02-19" NP732623.RAUOY8fcqyQRie-i8UbnDkr9zs6V5m_e4KNSlwlE1Czns130_provenance.