Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion> ?p ?o ?g. }
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- NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion type Assertion NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_head.
- NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion description "[Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant disease characterized by arteriovenous malformations and resulting from mutations in two major genes: ENG and ACVRL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_provenance.
- NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion evidence source_evidence_literature NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_provenance.
- NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion SIO_000772 16705692 NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_provenance.
- NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion wasDerivedFrom befree-20140225 NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_provenance.
- NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_assertion wasGeneratedBy ECO_0000203 NP439156.RAJsnYisTcUKNsO3CjJgpGs5r3Rvft_vD9QnG7qX10_t4130_provenance.