Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion> ?p ?o ?g. }
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- NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion type Assertion NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_head.
- NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion wasGeneratedBy ECO_0000218 NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_provenance.
- NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion wasDerivedFrom ctd_human-2016 NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_provenance.
- NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion SIO_000772 17704776 NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_provenance.
- NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion evidence source_evidence_curated NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_provenance.
- NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_assertion description "[Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20405.RArktynrsi9aMsG8E6qRAwTceoMrzZkQCSw3BbmxmJ4SE130_provenance.