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- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion type Assertion NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_head.
- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion wasGeneratedBy ECO_0000203 NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_provenance.
- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion wasDerivedFrom befree-2016 NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_provenance.
- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion SIO_000772 19508727 NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_provenance.
- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion evidence source_evidence_literature NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_provenance.
- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion description "[The genotype-phenotype correlation was consistent with a higher 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." NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_provenance.