Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion> ?p ?o ?g. }
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- NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion type Assertion NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_head.
- NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_provenance.
- NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion evidence source_evidence_literature NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_provenance.
- NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion SIO_000772 16542389 NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_provenance.
- NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion wasDerivedFrom befree-2016 NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_provenance.
- NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion wasGeneratedBy ECO_0000203 NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_provenance.