Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_assertion> ?p ?o ?g. }
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- NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_assertion type Assertion NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_head.
- NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_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." NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_provenance.
- NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_assertion evidence source_evidence_literature NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_provenance.
- NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_assertion SIO_000772 12920067 NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_provenance.
- NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_assertion wasDerivedFrom gad-20150221 NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_provenance.
- NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_assertion wasGeneratedBy ECO_0000203 NP60601.RArrhxL1E1LG9oxaP1FkuUHBuHvoin-096JS4L5CVeuA0130_provenance.