Matches in Nanopublications for { ?s ?p "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP564545.RAnRYa70sCV5iQ3CLz40No1frBYFOqSYbhUxzxka1F6iU130_assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP564545.RAnRYa70sCV5iQ3CLz40No1frBYFOqSYbhUxzxka1F6iU130_provenance.
- NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569594.RAin8vA84b3HBSNJlpcRIwL4tBqOb1YR8dWzjVxCZ6cgc130_provenance.
- assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP818713.RAs7RgGIwdPS5DSxKOPUKMJG4911aVuUCU1Grv_zH2Yds130_assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818713.RAs7RgGIwdPS5DSxKOPUKMJG4911aVuUCU1Grv_zH2Yds130_provenance.
- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.