Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion> ?p ?o ?g. }
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- NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion type Assertion NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_head.
- NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion description "[Mutations in endoglin (ENG) and activin-like kinase (ALK1) cause hereditary hemorrhagic telangiectasias, disorders characterized by pulmonary and brain arteriovenous malformations (BAVMs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_provenance.
- NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion evidence source_evidence_literature NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_provenance.
- NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion SIO_000772 16179574 NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_provenance.
- NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion wasDerivedFrom befree-20150227 NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_provenance.
- NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_assertion wasGeneratedBy ECO_0000203 NP222364.RAv0bUGh4z7MTj54j26Tzpl7vIyCSiTgOm715k2480_ng130_provenance.