Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_assertion> ?p ?o ?g. }
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- NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_assertion type Assertion NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_head.
- NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_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." NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_provenance.
- NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_assertion evidence source_evidence_literature NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_provenance.
- NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_assertion SIO_000772 19073947 NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_provenance.
- NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_assertion wasDerivedFrom befree-20150227 NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_provenance.
- NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_assertion wasGeneratedBy ECO_0000203 NP406882.RAxSAzVvCZdWLIvb59mevAmyQtv-o3SQJY0_zYK-LSXRc130_provenance.