Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion> ?p ?o ?g. }
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- NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion type Assertion NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_head.
- NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion description "[The association of the rare C4B3 variant with microangiopathy suggests a genetic component of its aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_provenance.
- NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion evidence source_evidence_literature NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_provenance.
- NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion SIO_000772 3926068 NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_provenance.
- NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion wasDerivedFrom befree-20140225 NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_provenance.
- NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_assertion wasGeneratedBy ECO_0000203 NP714476.RAxHeXwqNpVUGwsOXlf7ChiEXHQ2rTdpgV2x0IE4Zu2MU130_provenance.