Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion> ?p ?o ?g. }
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- NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion type Assertion NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_head.
- NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion description "[Mutations in two genes, endoglin and ALK-1, are known to cause HHT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_provenance.
- NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion evidence source_evidence_literature NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_provenance.
- NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion SIO_000772 10899246 NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_provenance.
- NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion wasDerivedFrom befree-20140225 NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_provenance.
- NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_assertion wasGeneratedBy ECO_0000203 NP194958.RAmZgY9zmS765wqpJTnkZhHzp1S0b2r7L80YbhT1PyCFw130_provenance.