Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP81241.RAqsCP-7ucFG3uU8NUPUhckzbGML_nzlzDq7tE3fDo7GE130_provenance.