| 000 | 01494 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250514155427.0 | ||
| 264 | 0 | _c20040317 | |
| 008 | 200403s 0 0 eng d | ||
| 022 | _a1367-4803 | ||
| 024 | 7 |
_a10.1093/bioinformatics/btg241 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMooney, Sean D | |
| 245 | 0 | 0 |
_aMutDB: annotating human variation with functionally relevant data. _h[electronic resource] |
| 260 |
_bBioinformatics (Oxford, England) _cSep 2003 |
||
| 300 |
_a1858-60 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aDatabase Management Systems |
| 650 | 0 | 4 | _aDatabases, Genetic |
| 650 | 0 | 4 | _aDatabases, Protein |
| 650 | 0 | 4 |
_aDocumentation _xmethods |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aGenetic Variation _xgenetics |
| 650 | 0 | 4 | _aGenome, Human |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInformation Storage and Retrieval _xmethods |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aProteins _xchemistry |
| 650 | 0 | 4 |
_aSequence Alignment _xmethods |
| 650 | 0 | 4 |
_aSequence Analysis, Protein _xmethods |
| 650 | 0 | 4 | _aStructure-Activity Relationship |
| 700 | 1 | _aAltman, Russ B | |
| 773 | 0 |
_tBioinformatics (Oxford, England) _gvol. 19 _gno. 14 _gp. 1858-60 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/bioinformatics/btg241 _zAvailable from publisher's website |
| 999 |
_c14273108 _d14273108 |
||