Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion> ?p ?o ?g. }
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- NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion type Assertion NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_head.
- NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion description "[Mutations in FLNA (Xq28) and ARFGEF2 (20q13) are responsible for X-linked bilateral PH and a rare autosomal recessive form of PH with microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_provenance.
- NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion evidence source_evidence_literature NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_provenance.
- NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion SIO_000772 19073947 NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_provenance.
- NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion wasDerivedFrom befree-2016 NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_provenance.
- NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_assertion wasGeneratedBy ECO_0000203 NP708459.RA2BdTP_vPsJlhtVL17cONc4_uvRiEUXt3odjGF0iXFqo130_provenance.