Ptpn11<tm7Bgn>

http://metadb.riken.jp/db/mgi_rdf/MGI:3840251

Ptpn11<tm7Bgn>

MGIアレル

synonym

http://metadb.riken.jp/db/mgi_rdf/allele_synonym

• ND
• Ptpn11<tm2.1Toa>
• Ptpn11<N308D>

アレルシンボル

http://www.w3.org/2000/01/rdf-schema#label

• Ptpn11<tm7Bgn>

MGI Accession ID

http://metadb.riken.jp/db/mgi_rdf/MGI_ID

• MGI:3840251

Allele Name

http://metadb.riken.jp/db/mgi_rdf/Allele_Name

• targeted mutation 7, Benjamin Neel

Allele Type

http://metadb.riken.jp/db/mgi_rdf/type_of_allele

• Targeted
  http://metadb.riken.jp/db/mgi_rdf/AlleleType/013

Allele Attribute

http://metadb.riken.jp/db/mgi_rdf/Allele_attribute

• Not Specified

PubMed ID for original reference

http://purl.org/net/cito/citesAsAuthority

• Toshiyuki. Araki, et.al., Noonan syndrome cardiac defects are caused by PTPN11 acting in endocardium to enhance endocardial-mesenchymal transformation., Proceedings of the National Academy of Sciences of the United States of America, 2009, 106
  http://rdf.ncbi.nlm.nih.gov/pubmed/19251646

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• protein tyrosine phosphatase, non-receptor type 11
  http://metadb.riken.jp/db/mgi_rdf/MGI:99511

Mutant Cell Line IDs

http://metadb.riken.jp/db/mgi_rdf/mutant_cell_line_id

See also (jump to original page)

http://www.w3.org/2000/01/rdf-schema#seeAlso

• http://identifiers.org/mgd/MGI:3840251

logical db name

http://metadb.riken.jp/db/mgi_rdf/project