Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion type Assertion NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_head.
- NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion description "[The vascular disorder Hereditary Hemorrhagic Telangiectasia (HHT) is in general an inherited disease caused by mutations in the TGF-?/BMP receptors endoglin or ALK1 or in rare cases by mutations of the TGF-? signal transducer protein Smad4 leading to the combined syndrome of juvenile polyposis and HHT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_provenance.
- NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion evidence source_evidence_literature NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_provenance.
- NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion SIO_000772 23805858 NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_provenance.
- NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion wasDerivedFrom befree-20140225 NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_provenance.
- NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_assertion wasGeneratedBy ECO_0000203 NP822680.RARO4SwyU1UE-IvQ92Vs_i1WDtlBYu_kwZ1Zmc6mPM-po130_provenance.