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- NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_assertion type Assertion NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_head.
- NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_assertion description "[Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_assertion evidence source_evidence_literature NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_assertion SIO_000772 12920067 NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_assertion wasDerivedFrom gad-20150221 NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_assertion wasGeneratedBy ECO_0000203 NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.