Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676930.RADt1eAkN8DRUQF4E6WHxoWSzfbMIIC9pOXD6BYTfP0Bg130_provenance.
• NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796079.RAiKJkCkx49VnRzNRMmLYmGHkzWDSYkBZL-g_Aa-cRKWc130_provenance.
• NP806717.RAVKpKaIkcUgUrJGTzeBx7TktPs0U-gvAmLuCm6Nhobuc130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806717.RAVKpKaIkcUgUrJGTzeBx7TktPs0U-gvAmLuCm6Nhobuc130_provenance.
• NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806967.RATHlFBV73DkpMcgb5Zm947k0NHkVLtak1ES1X5N8fAGY130_provenance.
• assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP670737.RAdAE3h2jgnk-zf2cck_4Tpad6aECApNtVPisJYsmzf6A130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670737.RAdAE3h2jgnk-zf2cck_4Tpad6aECApNtVPisJYsmzf6A130_provenance.
• NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
• NP670739.RAsWr8L1k_r_GuHPhgObYaYJ93Hof3Do8HKu1anTTM58s130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670739.RAsWr8L1k_r_GuHPhgObYaYJ93Hof3Do8HKu1anTTM58s130_provenance.
• NP806710.RAP6028qcXyuMVu5nQcpNnwu9bbkbDUMVM8g84GwJgyl4130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806710.RAP6028qcXyuMVu5nQcpNnwu9bbkbDUMVM8g84GwJgyl4130_provenance.
• NP806959.RAPimhFSoTWz0-PgzEnnEKbeaCMAytDC3Nx8dkUTu6CpM130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806959.RAPimhFSoTWz0-PgzEnnEKbeaCMAytDC3Nx8dkUTu6CpM130_provenance.