Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion> ?p ?o ?g. }
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- NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion type Assertion NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_head.
- NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_provenance.
- NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion evidence source_evidence_literature NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_provenance.
- NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion SIO_000772 19131948 NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_provenance.
- NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion wasDerivedFrom gad-20130706 NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_provenance.
- NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_assertion wasGeneratedBy ECO_0000203 NP74418.RA7P5B4Rr8mNlgLsnifq9Jrp8WUYPKm5_YPjcpzjt72lI130_provenance.