Matches in Nanopublications for { ?s ?p "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP755588.RAAtZbiasbGAuiJf9IDUfRcNrgFFiXTej9CoiKzrS5nFo130_assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755588.RAAtZbiasbGAuiJf9IDUfRcNrgFFiXTej9CoiKzrS5nFo130_provenance.
- NP775955.RAfYkiGBpm0ae4qxkqRKMP-Lc52k7e9Gn3Kkn_j0sqg4M130_assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775955.RAfYkiGBpm0ae4qxkqRKMP-Lc52k7e9Gn3Kkn_j0sqg4M130_provenance.
- NP476982.RAkUGW65xpEmfBE_O4rh9Q254N_r7NeILn0XDDccDC28I130_assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476982.RAkUGW65xpEmfBE_O4rh9Q254N_r7NeILn0XDDccDC28I130_provenance.
- NP442602.RA1WRMgy55JZeEnstmFSzOkLQHvTImkNJWdhffmKVmMUc130_assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442602.RA1WRMgy55JZeEnstmFSzOkLQHvTImkNJWdhffmKVmMUc130_provenance.
- NP603236.RA1URy4s1I2zkdJHYqUEDGdAuOrdJ56w66y7fVZOIN-8E130_assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603236.RA1URy4s1I2zkdJHYqUEDGdAuOrdJ56w66y7fVZOIN-8E130_provenance.
- assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP674031.RAm68lTU4bSvtFoRP7mfPmP0VuIFY-vUNJrREzxM7ZxFI130_assertion description "[OPHN1 mutations cause a syndromic form of mental retardation (MR) characterized by cerebellar hypoplasia, early hypotonia, motor and speech delay, with occasional seizures and strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674031.RAm68lTU4bSvtFoRP7mfPmP0VuIFY-vUNJrREzxM7ZxFI130_provenance.