Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion> ?p ?o ?g. }
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- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion type Assertion NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_head.
- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_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." NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_provenance.
- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion evidence source_evidence_literature NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_provenance.
- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion SIO_000772 19369868 NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_provenance.
- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion wasDerivedFrom befree-20140225 NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_provenance.
- NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_assertion wasGeneratedBy ECO_0000203 NP370615.RAR48C5Eg7_7Qp3ZQRdqMmej4xM3bp1U8eBKEaPLqpVLE130_provenance.